Modulation of diacylglycerol acyltransferase 2 expression

ABSTRACT

Compounds, compositions and methods are provided for modulating the expression of diacylglycerol acyltransferase 2. The compositions comprise oligonucleotides, targeted to nucleic acid encoding diacylglycerol acyltransferase 2. Methods of using these compounds for modulation of diacylglycerol acyltransferase 2 expression and for diagnosis and treatment of diseases and conditions associated with expression of diacylglycerol acyltransferase 2 are provided.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.12/748,281, filed Mar. 26, 2010, which is a divisional of U.S.application Ser. No. 11/066,725, filed Aug. 24, 2005, now issued as U.S.Pat. No. 7,732,590; which is a continuation of International ApplicationNo. PCT/US2004/024384, filed Aug. 18, 2004, which claims priority toU.S. application Ser. No. 10/643,801, filed Aug. 18, 2003, now issued asU.S. Pat. No. 7,825,235, the entire contents of each of the aboveapplications is herein incorporated by reference.

SEQUENCE LISTING

The present application is being filed along with a Sequence Listing inelectronic format. The Sequence Listing is provided as a file entitledRTS0678USC2SEQ.txt, created on Aug. 2, 2012 which is 164 Kb in size. Theinformation in the electronic format of the sequence listing isincorporated herein by reference in its entirety.

FIELD OF THE INVENTION

The present invention provides compositions and methods for modulatingthe expression of diacylglycerol acyltransferase 2. In particular, thisinvention relates to antisense compounds, particularly oligonucleotidecompounds, which, in preferred embodiments, hybridize with nucleic acidmolecules encoding diacylglycerol acyltransferase 2. Such compounds areshown herein to modulate the expression of diacylglycerolacyltransferase 2.

BACKGROUND OF THE INVENTION

Triglycerides are one of the major energy storage molecules ineukaryotes. The absorption of triglycerides (also calledtriacylglycerols) from food is a very efficient process which occurs bya series of steps wherein the dietary triacylglycerols are hydrolyzed inthe intestinal lumen and then resynthesized within enterocytes. Theresynthesis of triacylglycerols can occur via the monoacylglycerolpathwaywhich commences with monoacylglycerol acyltransferase (MGAT)catalyzing the synthesis of diacylglycerol from monoacylglycerol andfatty acyl-CoA. An alternative synthesis of diacylglycerols is providedby the glycerol-phosphate pathway which describes the coupling of twomolecules of fatty acyl-CoA to glycerol-3-phosphate. In either case,diacylglycerol is then acylated with another molecule of fatty acyl-CoAin a reaction catalyzed by one of two diacylglycerol acyltransferaseenzymes to form the triglyceride (Farese et al., Curr. Opin. Lipidol.,2000, 11, 229-234).

The reaction catalyzed by diacylglycerol acyltransferase is the finaland only committed step in triglyceride synthesis. As such,diacylglycerol acyltransferase is involved in intestinal fat absorption,lipoprotein assembly, regulating plasma triglyceride concentrations, andfat storage in adipocytes. The first diacylglycerol acyltransferase,diacylglycerol transferase 1, was identified in 1960 and the human andmouse genes encoding this protein were isolated in 1998 (Cases et al.,Proc. Natl. Acad. Sci. U.S.A., 1998, 95, 13018-13023; Oelkers et al., J.Biol. Chem., 1998, 273, 26765-26771). Mice lacking diacylglycerolacyltransferase 1 are viable and can still synthesize triglyceridesthrough other biological routes, suggesting the existence of multiplemechanisms for triglyceride synthesis (Smith et al., Nat. Genet., 2000,25, 87-90).

A second diacylglycerol transferase, diacylglycerol transferase 2 (alsoknown as DGAT2, diacylglycerol O-transferase 2, acyl-CoA:diacylglycerolacyltransferase 2), was subsequently identified in the fungusMortierella, humans and mice (Cases et al., J. Biol. Chem., 2001, 276,38870-38876; Lardizabal et al., J. Biol. Chem., 2001, 276, 38862-38869).Enzymatic assays indicate that this recently identified protein doespossess diacylglycerol transferase activity that utilizes a broad rangeof long chain fatty acyl-CoA substrates (Cases et al., J. Biol. Chem.,2001, 276, 38870-38876).

Diacylglycerol transferase 2 is a member of a family of genes whosesequences are unrelated to diacylglycerol transferase 1. In addition todiffering in sequence compared to diacylglycerol transferase 1, in vitroassays illustrate that diacylglycerol transferase 2 has higher activityat lower concentrations of magnesium chloride and oleoyl-CoA (Cases etal., J. Biol. Chem., 2001, 276, 38870-38876). The predicted proteinsequence of diacylglycerol transferase 2 contains at least one putativetransmembrane domain, three potential N-linked glycosylation sites, sixpotential protein kinase C phosphorylation consensus sites, as well assequences in common with a putative glycerol phosphorylation site foundin acyltransferase enzymes (Cases et al., J. Biol. Chem., 2001, 276,38870-38876). The International Radiation Hybrid Mapping Consortium hasmapped human diacylglycerol transferase 2 to chromosome 11q13.3.

In human tissues, the highest levels of diacylglycerol transferase 2 aredetected in liver and white adipose tissues, with lower levels found inmammary gland, testis and peripheral blood leukocytes (Cases et al., J.Biol. Chem., 2001, 276, 38870-38876). Two mRNA species of 2.4 and 1.8kilobases are detected in human tissues, whereas the majordiacylglycerol transferase 2 mRNA species in mouse tissues is 2.4kilobases. In addition to liver and white adipose tissues,diacylglycerol transferase 2 is expressed in all segments of the smallintestine in mice, with higher expression in the proximal intestine andlower expression in the distal intestine (Cases et al., J. Biol. Chem.,2001, 276, 38870-38876).

Diacylglycerol transferase activity exhibits distinct patterns duringpostnatal development of the rat liver. As there is no correlationbetween the mRNA expression and activity patterns, post-translationalmodifications may participate in the regulation of diacylglyceroltransferase 2 activity during rat development (Waterman et al., J.Lipid. Res., 2002, 43, 1555-1562).

Diacylglycerol transferase 2 mRNA is preferentially upregulated byinsulin treatment, as shown by in vitro assays measuring thediacylglycerol activity from the membrane fraction of cultured mouseadipocytes (Meegalla et al., Biochem. Biophys. Res. Commun., 2002, 298,317-323). In fasting mice, diacylglycerol transferase 2 expression isgreatly reduced, and dramatically increases upon refeeding. Theexpression patterns of two enzymes that participate in fatty acidsynthesis, acetyl-CoA carboxylase and fatty acid synthase, respond tofasting and refeeding in a similar fashion. These results, combined withthe observation that diacylglycerol transferase 2 is abundantlyexpressed in liver, suggest that diacylglycerol transferase 2 is tightlylinked to the endogenous fatty acid synthesis pathway (Meegalla et al.,Biochem. Biophys. Res. Commun., 2002, 298, 317-323).

Studies of mice harboring a disruption in the diacylglycerolacyltransferase 1 gene provide evidence that diacylglycerolacyltransferase 2 contributes to triglyceride synthesis. Levels ofdiacylglycerol transferase 2 mRNA expression are similar in intestinalsegments from both wild type and diacylglycerol transferase 1-deficientmice (Buhman et al., J. Biol. Chem., 2002, 277, 25474-25479). Usingmagnesium chloride to distinguish between diacylglycerol transferase 1and 2 activity, Buhman, et al. observed that, in diacylglyceroltransferase 1-deficient mice, diacylglycerol transferase activity isreduced to 50% in the proximal intestine and to 10-15% in the distalintestine (Buhman et al., J. Biol. Chem., 2002, 277, 25474-25479).

Additionally, diacylglycerol transferase 2 mRNA levels are notup-regulated the liver or adipose tissues of diacylglycerol transferase1-deficient mice, even after weeks of high-fat diet (Cases et al., J.Biol. Chem., 2001, 276, 38870-38876; Chen et al., J. Clin. Invest.,2002, 109, 1049-1055). However, in ob/ob mice, which have a mutation inthe leptin gene that results in obesity, diacylglycerol transferase 2 ismore highly expressed than in wild type mice, suggesting thatdiacylglycerol transferase 2 may be partly responsible for the highlyaccumulated fat mass seen in these mice. Furthermore, the combinedmutations of leptin and diacylglycerol transferase 1 leads to athree-fold elevation in diacylglycerol transferase 2 expression in whiteadipose tissue, compared to the levels in the same tissue fromdiacylglycerol transferase 1-deficient mice (Chen et al., J. Clin.Invest., 2002, 109, 1049-1055). Diacylglycerol transferase 2 mRNA isalso upregulated in the skin of these mice (Chen et al., J. Clin.Invest., 2002, 109, 175-181). These data suggest leptin normallydownregulates diacylglycerol transferase 2 expression, and that theupregulation of diacylglycerol transferase 2 in white adipose tissue inthese mice may provide an alternate pathway for the triglyceridesynthesis that still occurs in leptin deficient/diacylglyceroltransferase 1-deficient mice (Chen et al., J. Clin. Invest., 2002, 109,1049-1055).

Diacylglycerol acyltransferase 1 knockout mice exhibit interestingphenotypes in that they are lean, resistant to diet-induce obesity, havedecreased levels of tissue triglycerides and increased sensitivity toinsulin and leptin (Chen et al., J. Clin. Invest., 2002, 109, 1049-1055;Smith et al., Nat. Genet., 2000, 25, 87-90). As diacylglyceroltransferase 2 also participates in triglyceride synthesis, interferingwith diacylglycerol transferase 2 may similarly lead to reduced body fatcontent.

The US pre-grant publications 20030124126 and 20020119138 claim anddisclose a nucleic acid molecule encoding human diacylglyceroltransferase 2 alpha, as well as compositions, including antisenseoligonucleotides, for modulating the activity of said diacylglyceroltransferase 2 alpha (Cases et al., 2003).

The US pre-grant publication 20030104414 refers to nucleic acidsequences which are members of a group of genes referred to as “proteincluster V” as well as the method for identification of an agent capableof modulating nucleic acid molecules in the protein cluster V group.This application also refers to the use of RNA interference ordouble-stranded RNA to disrupt the function of protein cluster V genefamily members (Attersand, 2003).

The US pre-grant publication 20030100480 refers to modifyingdiacylglycerol transferase activity, including that of diacylglyceroltransferase 2, by a variety of methods, including antisense, RNAinterference and diacylglycerol transferase 2 antisense plasmidconstructs (Smith et al., 2003).

The US pre-grant publication 20030028923 refers to a method formodifying the triacylglycerol composition in a plant cell, comprisingtransforming a plant cell with a nucleic acid construct encoding anenzyme active in the formation of triacylglycerol from diacylglyceroland fatty acyl substrates, including nucleic acid constructs in theantisense orientation. Also referred to is a method for ameliorating adisease or condition associated with altered diacylglycerolacyltransferase activity by administering to a subject a therapeuticallyeffective amount of a diacylglycerol acyltransferase agonist. Thisapplication indicates that such antagonists can include antisensemolecules (Lardizabal et al., 2003).

The PCT publication WO 00/78961 refers to isolated nucleic acidmolecules selected from a group including a nucleic acid sequenceencoding diacylglycerol acyltransferase 2. This publication alsocomments that sense or antisense oligonucleotides binding to targetnucleic acid sequences can interfere with transcription or translationof the disclosed and claimed nucleic acid molecules (Baker et al.,2000).

The PCT publication WO 01/77389 refers to polynucleotides selected froma group of sequences including a nucleotide sequence encoding a humandiacylglycerol acyltransferase. A method for screening for the alteredexpression of said polynucleotides and a method for screening a libraryof molecules that specifically bind to said polynucleotide sequences arediscussed (Shiffman et al., 2001).

The PCT publication WO 01/68848 refers to a nucleic acid moleculesencoding secreted and transmembrane polypeptides, including a humandiacylglycerol acyltransferase 2 nucleic acid molecule, andoligonucleotide probes derived from any of these sequences (Baker etal., 2001).

European Patent Application No. EP 1 308 459 refers to a group ofpolynucleotide sequences, including a nucleic acid molecule encodinghuman diacylglycerol acyltransferase 2, and antisense polynucleotidesagainst this group of polynucleotide sequences (Isogai et al., 2003).

The PCT publication WO 02/08260 refers to an isolated, purifiedpolynucleotide sequence with identity to a human diacylglyceroltransferase 2 nucleotide sequence. This application also refers to asubstantially purified oligonucleotide that includes a region ofnucleotide sequence that hybridizes to at least 8 consecutivenucleotides of sense or antisense sequence of a nucleotide sequenceselected from a group consisting of sequences with identity to humandiacylglycerol acyltransferase 2 (Botstein et al., 2002).

Currently, there are no known therapeutic agents that effectivelyinhibit the synthesis of diacylglycerol acyltransferase 2. Consequently,there remains a long felt need for additional agents capable ofeffectively inhibiting diacylglycerol acyltransferase 2 function.

The present invention provides compositions and methods for modulatingdiacylglycerol acyltransferase 2 expression.

SUMMARY OF THE INVENTION

The present invention is directed to compounds, especially nucleic acidand nucleic acid-like oligomers, which are targeted to a nucleic acidencoding diacylglycerol acyltransferase 2, and which modulate theexpression of diacylglycerol acyltransferase 2. Pharmaceutical and othercompositions comprising the compounds of the invention are alsoprovided. Further provided are methods of screening for modulators ofdiacylglycerol acyltransferase 2 and methods of modulating theexpression of diacylglycerol acyltransferase 2 in cells, tissues oranimals comprising contacting said cells, tissues or animals with one ormore of the compounds or compositions of the invention.

Antisense technology is an effective means for reducing the expressionof specific gene products and may therefore prove to be uniquely usefulin a number of therapeutic, diagnostic, and research applications forthe modulation of diacylglycerol acyltransferase 2 expression.

Methods of treating an animal, particularly a human, suspected of havingor being prone to a disease or condition associated with expression ofdiacylglycerol acyltransferase 2 are also set forth herein. Such methodscomprise administering a therapeutically or prophylactically effectiveamount of one or more of the compounds or compositions of the inventionto the person in need of treatment.

In one aspect, the invention provides the use of a compound orcomposition of the invention in the manufacture of a medicament for thetreatment of any and all conditions disclosed herein.

DETAILED DESCRIPTION OF THE INVENTION

A. Overview of the Invention

The present invention employs antisense compounds, preferablyoligonucleotides and similar species for use in modulating the functionor effect of nucleic acid molecules encoding diacylglycerolacyltransferase 2. This is accomplished by providing oligonucleotidesthat specifically hybridize with one or more nucleic acid moleculesencoding diacylglycerol acyltransferase 2. As used herein, the terms“target nucleic acid” and “nucleic acid molecule encoding diacylglycerolacyltransferase 2” have been used for convenience to encompass DNAencoding diacylglycerol acyltransferase 2, RNA (including pre-mRNA andmRNA or portions thereof) transcribed from such DNA, and also cDNAderived from such RNA. The hybridization of a compound of this inventionwith its target nucleic acid is generally referred to as “antisense”.Consequently, the preferred mechanism believed to be included in thepractice of some preferred embodiments of the invention is referred toherein as “antisense inhibition.” Such antisense inhibition is typicallybased upon hydrogen bonding-based hybridization of oligonucleotidestrands or segments such that at least one strand or segment is cleaved,degraded, or otherwise rendered inoperable. In this regard, it ispresently preferred to target specific nucleic acid molecules and theirfunctions for such antisense inhibition.

The functions of DNA to be interfered with can include replication andtranscription. Replication and transcription, for example, can be froman endogenous cellular template, a vector, a plasmid construct orotherwise. The functions of RNA to be interfered with can includefunctions such as translocation of the RNA to a site of proteintranslation, translocation of the RNA to sites within the cell which aredistant from the site of RNA synthesis, translation of protein from theRNA, splicing of the RNA to yield one or more RNA species, and catalyticactivity or complex formation involving the RNA which may be engaged inor facilitated by the RNA. One preferred result of such interferencewith target nucleic acid function is modulation of the expression ofdiacylglycerol acyltransferase 2. In the context of the presentinvention, “modulation” and “modulation of expression” mean either anincrease (stimulation) or a decrease (inhibition) in the amount orlevels of a nucleic acid molecule encoding the gene, e.g., DNA or RNAInhibition is often the preferred form of modulation of expression andmRNA is often a preferred target nucleic acid.

In the context of this invention, “hybridization” means the pairing ofcomplementary strands of oligomeric compounds. In the present invention,the preferred mechanism of pairing involves hydrogen bonding, which maybe Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding,between complementary nucleoside or nucleotide bases (nucleobases) ofthe strands of oligomeric compounds. For example, adenine and thymineare complementary nucleobases which pair through the formation ofhydrogen bonds. Hybridization can occur under varying circumstances.

An antisense compound is specifically hybridizable when binding of thecompound to the target nucleic acid interferes with the normal functionof the target nucleic acid to cause a loss of activity, and there is asufficient degree of complementarity to avoid non-specific binding ofthe antisense compound to non-target nucleic acid sequences underconditions in which specific binding is desired, e.g., underphysiological conditions in the case of in vivo assays or therapeutictreatment, and under conditions in which assays are performed in thecase of in vitro assays.

In the present invention the phrase “stringent hybridization conditions”or “stringent conditions” refers to conditions under which a compound ofthe invention will hybridize to its target sequence, but to a minimalnumber of other sequences. Stringent conditions are sequence-dependentand will be different in different circumstances and in the context ofthis invention, “stringent conditions” under which oligomeric compoundshybridize to a target sequence are determined by the nature andcomposition of the oligomeric compounds and the assays in which they arebeing investigated.

“Complementary,” as used herein, refers to the capacity hydrogen bondingbetween the oligonucleotide and the target nucleic acid is considered tobe a complementary position. The oligonucleotide and the further DNA,RNA, or oligonucleotide molecule are complementary to each other when asufficient number of complementary positions in each molecule areoccupied by nucleobases which can hydrogen bond with each other. Thus,“specifically hybridizable” and “complementary” are terms which are usedto indicate a sufficient degree of precise pairing or complementarityover a sufficient number of nucleobases such that stable and specificbinding occurs between the oligonucleotide and a target nucleic acid.

It is understood in the art that the sequence of an antisense compoundmay be, but need not be, 100% complementary to that of its targetnucleic acid to be specifically hybridizable. Moreover, anoligonucleotide may hybridize over one or more segments such thatintervening or adjacent segments are not involved in the hybridizationevent (e.g., a loop structure or hairpin structure). It is preferredthat the antisense compounds of the present invention comprise at least70%, or at least 75%, or at least 80%, or at least 85% sequencecomplementarity to a target region within the target nucleic acid.Moreover, they may comprise at least 90% sequence complementarity, atleast 95% or at least 99% sequence complementarity to the target regionwithin the target nucleic acid sequence to which they are targeted. Forexample, an antisense compound in which 18 of 20 nucleobases of theantisense compound are complementary to a target region, and wouldtherefore specifically hybridize, would represent 90 percentcomplementarity. In this example, the remaining noncomplementarynucleobases may be clustered or interspersed with complementarynucleobases, and need not be contiguous to each other or tocomplementary nucleobases. As such, an antisense compound which is 18nucleobases in length having 4 (four) noncomplementary nucleobases whichare flanked by two regions of complete complementarity with the targetnucleic acid would have 77.8% overall complementarity with the targetnucleic acid and would thus fall within the scope of the presentinvention. Percent complementarity of an antisense compound with aregion of a target nucleic acid can be determined routinely using BLASTprograms (basic local alignment search tools) and PowerBLAST programsknown in the art (Altschul et al., J. Mol. Biol., 1990, 215, 403-410;Zhang and Madden, Genome Res., 1997, 7, 649-656).

Percent homology, sequence identity, or complementarity, can bedetermined by, for example, the Gap program (Wisconsin Sequence AnalysisPackage, Version 8 for Unix, Genetics Computer Group, UniversityResearch Park, Madison Wis.), using default settings, which uses thealgorithm of Smith and Waterman (Adv. Appl. Math., 1981, 2, 482-489). Insome preferred embodiments, homology, sequence identity, orcomplementarity, between the oligomeric compound and target is betweenabout 50% to about 60%. In some embodiments, homology, sequence identityor complementarity, is between about 60% to about 70%. In someembodiments, homology, sequence identity or complementarity, is betweenabout 70% and about 80%. In further embodiments, homology, sequenceidentity or complementarity, is between about 80% and about 90%. In someembodiments, homology, sequence identity or complementarity, is about90%, about 92%, about 94%, about 95%, about 96%, about 97%, about 98%,about 99% or about 100%.

B. Compounds of the Invention

According to the present invention, antisense compounds includeantisense oligomeric compounds, antisense oligonucleotides, siRNAs,external guide sequence (EGS) oligonucleotides, alternate splicers, andother oligomeric compounds which hybridize to at least a portion of thetarget nucleic acid. As such, these compounds may be introduced in theform of single-stranded, double-stranded, circular or hairpin oligomericcompounds and may contain structural elements such as internal orterminal bulges or loops. Once introduced to a system, the compounds ofthe invention may elicit the action of one or more enzymes or structuralproteins to effect modification of the target nucleic acid.

One non-limiting example of such an enzyme is RNase H, a cellularendonuclease which cleaves the RNA strand of an RNA:DNA duplex. It isknown in the art that single-stranded antisense compounds that are“DNA-like” elicit RNase H. Activation of RNase H, therefore, results incleavage of the RNA target, thereby greatly enhancing the efficiency ofoligonucleotide-mediated inhibition of gene expression. Similar roleshave been postulated for other ribonucleases such as those in the RNaseIII and ribonuclease L family of enzymes.

While the one form of antisense compound is a single-stranded antisenseoligonucleotide, in many species the introduction of double-strandedstructures, such as double-stranded RNA (dsRNA) molecules, has beenshown to induce potent and specific antisense-mediated reduction of thefunction of a gene or its associated gene products. This phenomenonoccurs in both plants and animals and is believed to have anevolutionary connection to viral defense and transposon silencing.

The first evidence that dsRNA could lead to gene silencing in animalscame in 1995 from work in the nematode, Caenorhabditis elegans (Guo andKempheus, Cell, 1995, 81, 611-620). The primary interference effects ofdsRNA are posttranscriptional (Montgomery et al., Proc. Natl. Acad. Sci.USA, 1998, 95, 15502-15507). The posttranscriptional antisense mechanismdefined in Caenorhabditis elegans resulting from exposure todouble-stranded RNA (dsRNA) has since been designated RNA interference(RNAi). This term has been generalized to mean antisense-mediated genesilencing involving the introduction of dsRNA leading to thesequence-specific reduction of endogenous targeted mRNA levels (Fire etal., Nature, 1998, 391, 806-811). Recently, the single-stranded RNAoligomers of antisense polarity of the dsRNAs have been reported to bethe potent inducers of RNAi (Tijsterman et al., Science, 2002, 295,694-697).

The antisense compounds of the present invention also include modifiedcompounds in which a different base is present at one or more of thenucleotide positions in the compound. For example, if the firstnucleotide is an adenosine, modified compounds may be produced whichcontain thymidine, guanosine or cytidine at this position. This may bedone at any of the positions of the antisense compound. These compoundsare then tested using the methods described herein to determine theirability to inhibit expression of diacylglycerol acyltransferase 2 mRNA.

In the context of this invention, the term “oligomeric compound” refersto a polymer or oligomer comprising a plurality of monomeric units. Inthe context of this invention, the term “oligonucleotide” refers to anoligomer or polymer of ribonucleic acid (RNA) or deoxyribonucleic acid(DNA) or mimetics, chimeras, analogs and homologs thereof. This termincludes oligonucleotides composed of naturally occurring nucleobases,sugars and covalent internucleoside (backbone) linkages as well asoligonucleotides having non-naturally occurring portions which functionsimilarly. Such modified or substituted oligonucleotides are oftenpreferred over native forms because of desirable properties such as, forexample, enhanced cellular uptake, enhanced affinity for a targetnucleic acid and increased stability in the presence of nucleases.

While oligonucleotides are a preferred form of the antisense compoundsof this invention, the present invention comprehends other families ofantisense compounds as well, including but not limited tooligonucleotide analogs and mimetics such as those described herein.

The antisense compounds in accordance with this invention preferablycomprise from about 8 to about 80 nucleobases (i.e. from about 8 toabout 80 linked nucleosides). One of ordinary skill in the art willappreciate that the invention embodies compounds of 8, 9, 10, 11, 12,13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30,31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48,49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66,67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, or 80 nucleobases inlength.

In one embodiment, the antisense compounds of the invention are 12 to 50nucleobases in length. One having ordinary skill in the art willappreciate that this embodies compounds of 12, 13, 14, 15, 16, 17, 18,19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36,37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50 nucleobases inlength.

In one embodiment, the antisense compounds of the invention are 13 to 40nucleobases in length. One having ordinary skill in the art willappreciate that this embodies compounds of 13, 14, 15, 16, 17, 18, 19,20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37,38, 39 or 40 nucleobases in length.

In another embodiment, the antisense compounds of the invention are 15to 30 nucleobases in length. One having ordinary skill in the art willappreciate that this embodies compounds of 15, 16, 17, 18, 19, 20, 21,22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleobases in length.

In further embodiments, the antisense compounds are oligonucleotidesfrom about 12 to about 50 nucleobases, or from about 13 to 40nucleobases, or from about 15 to about 30 nucleobases.

In another embodiment, the antisense compounds comprise at least 8contiguous nucleobases of an antisense compound disclosed herein.

Antisense compounds 8-80 nucleobases in length comprising a stretch ofat least eight (8) consecutive nucleobases selected from within theillustrative antisense compounds are considered to be suitable antisensecompounds as well.

Further antisense compounds include oligonucleotide sequences thatcomprise at least the 8 consecutive nucleobases from the 5′-terminus ofone of the illustrative preferred antisense compounds (the remainingnucleobases being a consecutive stretch of the same oligonucleotidebeginning immediately upstream of the 5′-terminus of the antisensecompound that is specifically hybridizable to the target nucleic acidand continuing until the oligonucleotide contains about 8 to about 80nucleobases). Similarly, antisense compounds are represented byoligonucleotide sequences that comprise at least the 8 consecutivenucleobases from the 3′-terminus of one of the illustrative preferredantisense compounds (the remaining nucleobases being a consecutivestretch of the same oligonucleotide beginning immediately downstream ofthe 3′-terminus of the antisense compound that is specificallyhybridizable to the target nucleic acid and continuing until theoligonucleotide contains about 8 to about 80 nucleobases). It is alsounderstood that antisense compounds may be represented byoligonucleotide sequences that comprise at least 8 consecutivenucleobases from an internal portion of the sequence of an illustrativepreferred antisense compound, and may extend in either or bothdirections until the oligonucleotide contains about 8 to about 80nucleobases.

In one embodiment, the antisense compound includes SEQ ID NOS: 20, 21,23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40,41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 56, 57, 58, 60,61, 62, 63, 64, 65, 66, 68, 69, 70, 71, 72, 73, 75, 76, 77, 78, 80, 81,82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 94, 95, 96, 97, 101, 109,114, 115, 120, 121, 122, 123, 124, 127, 128, 130, 133, 136 or 142. Instill other embodiments, the antisense compounds are one or more of SEQID NOS: 277 through 411.

In another embodiment, the antisense compound includes SEQ ID NOS: 21,24, 25, 26, 28, 29, 35, 36, 47, 49, 57, 62, 65, 66, 71, 73, 77, 81, 82,90, 92 or 94

One having skill in the art armed with the preferred antisense compoundsillustrated herein will be able, without undue experimentation, toidentify further preferred antisense compounds.

C. Targets of the Invention

“Targeting” an antisense compound to a particular nucleic acid molecule,in the context of this invention, can be a multistep process. Theprocess usually begins with the identification of a target nucleic acidwhose function is to be modulated. This target nucleic acid may be, forexample, a cellular gene (or mRNA transcribed from the gene) whoseexpression is associated with a particular disorder or disease state, ora nucleic acid molecule from an infectious agent. In the presentinvention, the target nucleic acid encodes diacylglycerolacyltransferase 2.

The targeting process usually also includes determination of at leastone target region, segment, or site within the target nucleic acid forthe antisense interaction to occur such that the desired effect, e.g.,modulation of expression, will result. Within the context of the presentinvention, the term “region” is defined as a portion of the targetnucleic acid having at least one identifiable structure, function, orcharacteristic. Within regions of target nucleic acids are segments.“Segments” are defined as smaller or sub-portions of regions within atarget nucleic acid. “Sites,” as used in the present invention, aredefined as positions within a target nucleic acid.

Since, as is known in the art, the translation initiation codon istypically 5′-AUG (in transcribed mRNA molecules; 5′-ATG in thecorresponding DNA molecule), the translation initiation codon is alsoreferred to as the “AUG codon,” the “start codon” or the “AUG startcodon”. A minority of genes having a translation initiation codon withthe RNA sequence 5′-GUG, 5′-UUG or 5′-CUG, and 5′-AUA, 5′-ACG and 5′-CUGhave been shown to function in vivo. Thus, the terms “translationinitiation codon” and “start codon” can encompass many codon sequences,even though the initiator amino acid in each instance is typicallymethionine (in eukaryotes) or formylmethionine (in prokaryotes). It isalso known in the art that eukaryotic and prokaryotic genes may have twoor more alternative start codons, any one of which may be preferentiallyutilized for translation initiation in a particular cell type or tissue,or under a particular set of conditions. In the context of theinvention, “start codon” and “translation initiation codon” refer to thecodon or codons that are used in vivo to initiate translation of an mRNAtranscribed from a gene encoding diacylglycerol acyltransferase 2,regardless of the sequence(s) of such codons. It is also known in theart that a translation termination codon (or “stop codon”) of a gene mayhave one of three sequences, i.e., 5′-UAA, 5′-UAG and 5′-UGA (thecorresponding DNA sequences are 5′-TAA, 5′-TAG and 5′-TGA,respectively).

The terms “start codon region” and “translation initiation codon region”refer to a portion of such an mRNA or gene that encompasses from about25 to about 50 contiguous nucleotides in either direction (i.e., 5′ or3′) from a translation initiation codon. Similarly, the terms “stopcodon region” and “translation termination codon region” refer to aportion of such an mRNA or gene that encompasses from about 25 to about50 contiguous nucleotides in either direction (i.e., 5′ or 3′) from atranslation termination codon. Consequently, the “start codon region”(or “translation initiation codon region”) and the “stop codon region”(or “translation termination codon region”) are all regions which may betargeted effectively with the antisense compounds of the presentinvention.

The open reading frame (ORF) or “coding region,” which is known in theart to refer to the region between the translation initiation codon andthe translation termination codon, is also a region which may betargeted effectively. Within the context of the present invention, apreferred region is the intragenic region encompassing the translationinitiation or termination codon of the open reading frame (ORF) of agene.

Other target regions include the 5′ untranslated region (5′UTR), knownin the art to refer to the portion of an mRNA in the 5′ direction fromthe translation initiation codon, and thus including nucleotides betweenthe 5′ cap site and the translation initiation codon of an mRNA (orcorresponding nucleotides on the gene), and the 3′ untranslated region(3′UTR), known in the art to refer to the portion of an mRNA in the 3′direction from the translation termination codon, and thus includingnucleotides between the translation termination codon and 3′ end of anmRNA (or corresponding nucleotides on the gene). The 5′ cap site of anmRNA comprises an N7-methylated guanosine residue joined to the 5′-mostresidue of the mRNA via a 5′-5′ triphosphate linkage. The 5′ cap regionof an mRNA is considered to include the 5′ cap structure itself as wellas the first 50 nucleotides adjacent to the cap site. It is alsopreferred to target the 5′ cap region.

Accordingly, the present invention provides antisense compounds thattarget a portion of nucleotides 1-2439 as set forth in SEQ ID NO: 4. Inanother embodiment, the antisense compounds target at least an8-nucleobase portion of nucleotides 1-230, comprising the 5′UTR as setforth in SEQ ID NO: 4. In another embodiment, the antisense compoundstarget at least an 8-nucleobase portion of nucleotides 1395-2439,comprising the 3′UTR as set forth in SEQ ID NO: 4. In anotherembodiment, the antisense compounds target at least an 8-nucleobaseportion of nucleotides 231-1394, comprising the coding region as setforth in SEQ ID NO: 4. In still other embodiments, the antisensecompounds target at least an 8-nucleobase portion of a “preferred targetsegment” (as defined herein) as set forth in Table 3 or additionalTables in the Examples below.

Although some eukaryotic mRNA transcripts are directly translated, manycontain one or more regions, known as “introns,” which are excised froma transcript before it is translated. The remaining (and thereforetranslated) regions are known as “exons” and are spliced together toform a continuous mRNA sequence, resulting in exon-exon junctions at thesites where exons are joined. Targeting exon-exon junctions can beuseful in situations where the overproduction of a normal splice productis implicated in disease, or where the overproduction of an aberrantsplice product is implicated in disease. Targeting splice sites, i.e.,intron-exon junctions or exon-intron junctions, may also be particularlyuseful in situations where aberrant splicing is implicated in disease,or where an overproduction of a particular splice product is implicatedin disease. Aberrant fusion junctions due to rearrangements or deletionsare also preferred target sites. mRNA transcripts produced via theprocess of splicing of two (or more) mRNAs from different gene sources,known as “fusion transcripts”, are also suitable target sites. It isalso known that introns can be effectively targeted using antisensecompounds targeted to, for example, DNA or pre-mRNA.

It is also known in the art that alternative RNA transcripts can beproduced from the same genomic region of DNA. These alternativetranscripts are generally known as “variants”. More specifically,“pre-mRNA variants” are transcripts produced from the same genomic DNAthat differ from other transcripts produced from the same genomic DNA ineither their start or stop position and contain both intronic and exonicsequence.

Upon excision of one or more exon or intron regions, or portions thereofduring splicing, pre-mRNA variants produce smaller “mRNA variants”.Consequently, mRNA variants are processed pre-mRNA variants, and eachunique pre-mRNA variant must always produce a unique mRNA variant as aresult of splicing. These mRNA variants are also known as “alternativesplice variants”. If no splicing of the pre-mRNA variant occurs then thepre-mRNA variant is identical to the mRNA variant.

It is also known in the art that variants can be produced through theuse of alternative signals to start or stop transcription and thatpre-mRNAs and mRNAs can possess more that one start codon or stop codon.Variants that originate from a pre-mRNA or mRNA that use alternativestart codons are known as “alternative start variants” of that pre-mRNAor mRNA. Those transcripts that use an alternative stop codon are knownas “alternative stop variants” of that pre-mRNA or mRNA. One specifictype of alternative stop variant is the “polyA variant” in which themultiple transcripts produced result from the alternative selection ofone of the “polyA stop signals” by the transcription machinery, therebyproducing transcripts that terminate at unique polyA sites. Within thecontext of the invention, the types of variants described herein arealso preferred target nucleic acids.

The locations on the target nucleic acid to which the preferredantisense compounds hybridize are hereinbelow referred to as “preferredtarget segments.” As used herein the term “preferred target segment” isdefined as at least an 8-nucleobase portion of a target region to whichan active antisense compound is targeted. While not wishing to be boundby theory, it is presently believed that these target segments representportions of the target nucleic acid which are accessible forhybridization.

While the specific sequences of certain preferred target segments areset forth herein, one of skill in the art will recognize that theseserve to illustrate and describe particular embodiments within the scopeof the present invention. Additional preferred target segments may beidentified by one having ordinary skill.

Target segments 8-80 nucleobases in length comprising a stretch of atleast eight (8) consecutive nucleobases selected from within theillustrative preferred target segments are considered to be suitable fortargeting as well.

Target segments can include DNA or RNA sequences that comprise at leastthe 8 consecutive nucleobases from the 5′-terminus of one of theillustrative preferred target segments (the remaining nucleobases beinga consecutive stretch of the same DNA or RNA beginning immediatelyupstream of the 5′-terminus of the target segment and continuing untilthe DNA or RNA contains about 8 to about 80 nucleobases). Similarlypreferred target segments are represented by DNA or RNA sequences thatcomprise at least the 8 consecutive nucleobases from the 3′-terminus ofone of the illustrative preferred target segments (the remainingnucleobases being a consecutive stretch of the same DNA or RNA beginningimmediately downstream of the 3′-terminus of the target segment andcontinuing until the DNA or RNA contains about 8 to about 80nucleobases). It is also understood that preferred antisense targetsegments may be represented by DNA or RNA sequences that comprise atleast 8 consecutive nucleobases from an internal portion of the sequenceof an illustrative preferred target segment, and may extend in either orboth directions until the oligonucleotide contains about 8 to about 80nucleobases. One having skill in the art armed with the preferred targetsegments illustrated herein will be able, without undue experimentation,to identify further preferred target segments.

Once one or more target regions, segments or sites have been identified,antisense compounds are chosen which are sufficiently complementary tothe target, i.e., hybridize sufficiently well and with sufficientspecificity, to give the desired effect.

The oligomeric antisense compounds can also be targeted to regions of atarget nucleobase sequence, such as those disclosed herein (e.g., inExample 13) All regions of a nucleobase sequence to which an oligomericantisense compound can be targeted, wherein the regions are greater thanor equal to 8 and less than or equal to 80 nucleobases, are described asfollows:

Let R(m, n+m−1) be a region from a target nucleobase sequence, where “n”is the 5′-most nucleobase position of the region, where “n+m−1” is the3′-most nucleobase position of the region and where “m” is the length ofthe region. A set “S(m)”, of regions of length “m” is defined as theregions where n ranges from 1 to L−m+1, where L is the length of thetarget nucleobase sequence and L>m. A set, “A”, of all regions can beconstructed as a union of the sets of regions for each length from wherem is greater than or equal to 8 and is less than or equal to 80.

This set of regions can be represented using the following mathematicalnotation:

$A = \left. {{\bigcup\limits_{m}{{S(m)}\mspace{14mu} {where}\mspace{14mu} m}} \in N} \middle| {8 \leq m \leq 80} \right.$and S(m) = {R_(n, n + m − 1)|n ∈ {1, 2, 3, …  , L − m + 1}}

where the mathematical operator|indicates “such that”,

where the mathematical operator c indicates “a member of a set” (e.g.yεZ indicates that element y is a member of set Z),

where x is a variable,

where N indicates all natural numbers, defined as positive integers, andwhere the mathematical operator ∪ indicates “the union of sets”.

For example, the set of regions for m equal to 8, 20 and 80 can beconstructed in the following manner. The set of regions, each 8nucleobases in length, S(m=8), in a target nucleobase sequence 100nucleobases in length (L=100), beginning at position 1 (n=1) of thetarget nucleobase sequence, can be created using the followingexpression:

S(8)={R _(1,8) |nε{1,2,3, . . . ,93}}

and describes the set of regions comprising nucleobases 1-8, 2-9, 3-10,4-11, 5-12, 6-13, 7-14, 8-15, 9-16, 10-17, 11-18, 12-19, 13-20, 14-21,15-22, 16-23, 17-24, 18-25, 19-26, 20-27, 21-28, 22-29, 23-30, 24-31,25-32, 26-33, 27-34, 28-35, 29-36, 30-37, 31-38, 32-39, 33-40, 34-41,35-42, 36-43, 37-44, 38-45, 39-46, 40-47, 41-48, 42-49, 43-50, 44-51,45-52, 46-53, 47-54, 48-55, 49-56, 50-57, 51-58, 52-59, 53-60, 54-61,55-62, 56-63, 57-64, 58-65, 59-66, 60-67, 61-68, 62-69, 63-70, 64-71,65-72, 66-73, 67-74, 68-75, 69-76, 70-77, 71-78, 72-79, 73-80, 74-81,75-82, 76-83, 77-84, 78-85, 79-86, 80-87, 81-88, 82-89, 83-90, 84-91,85-92, 86-93, 87-94, 88-95, 89-96, 90-97, 91-98, 92-99, 93-100.

An additional set for regions 20 nucleobases in length, in a targetsequence 100 nucleobases in length, beginning at position 1 of thetarget nucleobase sequence, can be described using the followingexpression:

S(20)={R _(1,20) |nε{1,2,3, . . . ,81}}

and describes the set of regions comprising nucleobases 1-20, 2-21,3-22, 4-23, 5-24, 6-25, 7-26, 8-27, 9-28, 10-29, 11-30, 12-31, 13-32,14-33, 15-34, 16-35, 17-36, 18-37, 19-38, 20-39, 21-40, 22-41, 23-42,24-43, 25-44, 26-45, 27-46, 28-47, 29-48, 30-49, 31-50, 32-51, 33-52,34-53, 35-54, 36-55, 37-56, 38-57, 39-58, 40-59, 41-60, 42-61, 43-62,44-63, 45-64, 46-65, 47-66, 48-67, 49-68, 50-69, 51-70, 52-71, 53-72,54-73, 55-74, 56-75, 57-76, 58-77, 59-78, 60-79, 61-80, 62-81, 63-82,64-83, 65-84, 66-85, 67-86, 68-87, 69-88, 70-89, 71-90, 72-91, 73-92,74-93, 75-94, 76-95, 77-96, 78-97, 79-98, 80-99, 81-100.

An additional set for regions 80 nucleobases in length, in a targetsequence 100 nucleobases in length, beginning at position 1 of thetarget nucleobase sequence, can be described using the followingexpression:

S(80)={R _(1,20) |nε{1,2,3, . . . ,81}}

and describes the set of regions comprising nucleobases 1-80, 2-81,3-82, 4-83, 5-84, 6-85, 7-86, 8-87, 9-88, 10-89, 11-90, 12-91, 13-92,14-93, 15-94, 16-95, 17-96, 18-97, 19-98, 20-99, 21-100.

Thus, in this example, A would include regions 1-8, 2-9, 3-10 . . .93-100, 1-20, 2-21, 3-22 . . . 81-100, 1-80, 2-81, 3-82 . . . 21-100.

The union of these aforementioned example sets and other sets forlengths from 10 to 19 and 21 to 79 can be described using themathematical expression:

$A = {\bigcup\limits_{m}{S(m)}}$

where ∪ represents the union of the sets obtained by combining allmembers of all sets.

The mathematical expressions described herein define all possible targetregions in a target nucleobase sequence of any length L, where theregion is of length m, and where m is greater than or equal to 8 andless than or equal to 80 nucleobases, and where m is less than L, andwhere n is less than L−m+1.

D. Screening and Target Validation

In a further embodiment, the “preferred target segments” identifiedherein may be employed in a screen for additional compounds thatmodulate the expression of diacylglycerol acyltransferase 2.“Modulators” are those compounds that decrease or increase theexpression of a nucleic acid molecule encoding diacylglycerolacyltransferase 2 and which comprise at least an 8-nucleobase portionwhich is complementary to a preferred target segment. The screeningmethod comprises the steps of contacting a preferred target segment of anucleic acid molecule encoding diacylglycerol acyltransferase 2 with oneor more candidate modulators, and selecting for one or more candidatemodulators which decrease or increase the expression of a nucleic acidmolecule encoding diacylglycerol acyltransferase 2. Once it is shownthat the candidate modulator or modulators are capable of modulating(e.g. either decreasing or increasing) the expression of a nucleic acidmolecule encoding diacylglycerol acyltransferase 2, the modulator maythen be employed in further investigative studies of the function ofdiacylglycerol acyltransferase 2, or for use as a research, diagnostic,or therapeutic agent in accordance with the present invention.

The preferred target segments of the present invention may be also becombined with their respective complementary antisense compounds of thepresent invention to form stabilized double-stranded (duplexed)oligonucleotides.

Such double stranded oligonucleotide moieties have been shown in the artto modulate target expression and regulate translation as well as RNAprocessing via an antisense mechanism. Moreover, the double-strandedmoieties may be subject to chemical modifications (Fire et al., Nature,1998, 391, 806-811; Timmons and Fire, Nature 1998, 395, 854; Timmons etal., Gene, 2001, 263, 103-112; Tabara et al., Science, 1998, 282,430-431; Montgomery et al., Proc. Natl. Acad. Sci. USA, 1998, 95,15502-15507; Tuschl et al., Genes Dev., 1999, 13, 3191-3197; Elbashir etal., Nature, 2001, 411, 494-498; Elbashir et al., Genes Dev. 2001, 15,188-200). For example, such double-stranded moieties have been shown toinhibit the target by the classical hybridization of the antisensestrand of the duplex to the target, thereby triggering enzymaticdegradation of the target (Tijsterman et al., Science, 2002, 295,694-697).

The compounds of the present invention can also be applied in the areasof drug discovery and target validation. The present inventioncomprehends the use of the compounds and preferred target segmentsidentified herein in drug discovery efforts to elucidate relationshipsthat exist between diacylglycerol acyltransferase 2 and a disease state,phenotype, or condition. These methods include detecting or modulatingdiacylglycerol acyltransferase 2 comprising contacting a sample, tissue,cell, or organism with the compounds of the present invention, measuringthe nucleic acid or protein level of diacylglycerol acyltransferase 2and/or a related phenotypic or chemical endpoint at some time aftertreatment, and optionally comparing the measured value to a non-treatedsample or sample treated with a further compound of the invention. Thesemethods can also be performed in parallel or in combination with otherexperiments to determine the function of unknown genes for the processof target validation or to determine the validity of a particular geneproduct as a target for treatment or prevention of a particular disease,condition, or phenotype.

E. Kits, Research Reagents, Diagnostics, and Therapeutics

The antisense compounds of the present invention are utilized fordiagnostics, therapeutics, prophylaxis and as research reagents andkits. Furthermore, antisense oligonucleotides, which are able to inhibitgene expression with exquisite specificity, are often used by those ofordinary skill to elucidate the function of particular genes or todistinguish between functions of various members of a biologicalpathway.

For use in kits and diagnostics, the compounds of the present invention,either alone or in combination with other compounds or therapeutics, areused as tools in differential and/or combinatorial analyses to elucidateexpression patterns of a portion or the entire complement of genesexpressed within cells and tissues.

As one nonlimiting example, expression patterns within cells or tissuestreated with one or more antisense compounds are compared to controlcells or tissues not treated with antisense compounds and the patternsproduced are analyzed for differential levels of gene expression as theypertain, for example, to disease association, signaling pathway,cellular localization, expression level, size, structure or function ofthe genes examined. These analyses can be performed on stimulated orunstimulated cells and in the presence or absence of other compoundswhich affect expression patterns.

Examples of methods of gene expression analysis known in the art includeDNA arrays or microarrays (Brazma and Vilo, FEBS Lett., 2000, 480,17-24; Celis, et al., FEBS Lett., 2000, 480, 2-16), SAGE (serialanalysis of gene expression) (Madden, et al., Drug Discov. Today, 2000,5, 415-425), READS (restriction enzyme amplification of digested cDNAs)(Prashar and Weissman, Methods Enzymol., 1999, 303, 258-72), TOGA (totalgene expression analysis) (Sutcliffe, et al., Proc. Natl. Acad. Sci.U.S.A., 2000, 97, 1976-81), protein arrays and proteomics (Celis, etal., FEBS Lett., 2000, 480, 2-16; Jungblut, et al., Electrophoresis,1999, 20, 2100-10), expressed sequence tag (EST) sequencing (Celis, etal., FEBS Lett., 2000, 480, 2-16; Larsson, et al., J. Biotechnol., 2000,80, 143-57), subtractive RNA fingerprinting (SuRF) (Fuchs, et al., Anal.Biochem., 2000, 286, 91-98; Larson, et al., Cytometry, 2000, 41,203-208), subtractive cloning, differential display (DD) (Jurecic andBelmont, Curr. Opin. Microbiol., 2000, 3, 316-21), comparative genomichybridization (Carulli, et al., J. Cell Biochem. Suppl., 1998, 31,286-96), FISH (fluorescent in situ hybridization) techniques (Going andGusterson, Eur. J. Cancer, 1999, 35, 1895-904) and mass spectrometrymethods (To, Comb. Chem. High Throughput Screen, 2000, 3, 235-41).

The antisense compounds of the invention are useful for research anddiagnostics, because these compounds hybridize to nucleic acids encodingdiacylglycerol acyltransferase 2. The primers and probes disclosedherein are useful in methods requiring the specific detection of nucleicacid molecules encoding diacylglycerol acyltransferase 2 and in theamplification of said nucleic acid molecules for detection or for use infurther studies of diacylglycerol acyltransferase 2. Hybridization ofthe primers and probes with a nucleic acid encoding diacylglycerolacyltransferase 2 can be detected by means known in the art. Such meansmay include conjugation of an enzyme to the primer or probe or any othersuitable detection means. Kits using such detection means for detectingthe level of diacylglycerol acyltransferase 2 in a sample may also beprepared.

The invention further provides for the use of a compound or compositionof the invention in the manufacture of a medicament for the treatment ofany and all conditions disclosed herein.

The specificity and sensitivity of antisense are also harnessed by thoseof skill in the art for therapeutic uses. Antisense compounds have beenemployed as therapeutic moieties in the treatment of disease states inanimals, including humans. Antisense oligonucleotide drugs, includingribozymes, have been safely and effectively administered to humans andnumerous clinical trials are underway. It is thus established thatantisense compounds can be useful therapeutic modalities that can beconfigured to be useful in treatment regimes for the treatment of cells,tissues and animals, especially humans.

For therapeutics, an animal, preferably a human, suspected of having adisease or disorder which can be treated by modulating the expression ofdiacylglycerol acyltransferase 2 is treated by administering antisensecompounds in accordance with this invention. For example, in onenon-limiting embodiment, the methods comprise the step of administeringto the animal in need of treatment, a therapeutically effective amountof a diacylglycerol acyltransferase 2 inhibitor. The diacylglycerolacyltransferase 2 inhibitors of the present invention effectivelyinhibit the activity of the diacylglycerol acyltransferase 2 protein orinhibit the expression of the diacylglycerol acyltransferase 2 protein.In one embodiment, the activity or expression of diacylglycerolacyltransferase 2 in an animal is inhibited by about 10%. Preferably,the activity or expression of diacylglycerol acyltransferase 2 in ananimal is inhibited by about 30%. More preferably, the activity orexpression of diacylglycerol acyltransferase 2 in an animal is inhibitedby 50% or more. Thus, the antisense compounds modulate expression ofdiacylglycerol acyltransferase 2 mRNA by at least 10%, by at least 20%,by at least 25%, by at least 30%, by at least 40%, by at least 50%, byat least 60%, by at least 70%, by at least 75%, by at least 80%, by atleast 85%, by at least 90%, by at least 95%, by at least 98%, by atleast 99%, or by 100%.

For example, the reduction of the expression of diacylglycerolacyltransferase 2 may be measured in serum, adipose tissue, liver or anyother body fluid, tissue or organ of the animal. Preferably, the cellscontained within said fluids, tissues or organs being analyzed contain anucleic acid molecule encoding diacylglycerol acyltransferase 2 proteinand/or the diacylglycerol acyltransferase 2 protein itself.

The antisense compounds of the invention can be utilized inpharmaceutical compositions by adding an effective amount of a compoundto a suitable pharmaceutically acceptable diluent or carrier. Thecompounds and methods of the invention may also be usefulprophylactically.

The antisense compounds of the present invention are also useful foridentifying diseased states associated with diacylglycerolacyltransferase 2 expression. The methods include identifying thepresence of a nucleic acid encoding diacylglycerol acyltransferase 2 ina sample using at least one of the primers comprising SEQ ID NOs: 6 or7, or the probe comprising SEQ ID NO: 8.

The antisense compounds are further useful for treating or preventing avariety of conditions. Typically, the compounds of the present inventionare utilized to ameliorate or lessen the severity of a condition in ananimal. The conditions can include cardiovascular disorder, obesity suchas diet induced obesity, diabetes, cholesterolemia, and liver steatosis,among others. There are several physical indicia of obesity and includeincreased fat, among others. The treatment or prevention of a conditionusing the compounds of the invention can include contacting an animalwith an effective amount of a compound of the invention. Preferably,expression of diacylglycerol acyltransferase 2 is inhibited and themeasurement of one or more physical indicia of the condition indicates alessening of the severity of the condition. Typically, the animal isobese.

The antisense compounds are additionally utilized for lowering certaincomponents of blood from an animal. Typically, the compounds of theinvention are useful for lowering serum free fatty acids, serumtriglycerides, lowering HDL cholesterol, lowering total serumcholesterol, plasma or serum insulin, or hepatic triglycerides in ananimal. Typically, the animal is contacted with an effective amount of acompound of the invention. Preferably, the plasma insulin levels arelowered at about two or four weeks after contacting the animal with acompound of the invention.

The compounds of the invention are also useful in inhibiting theexpression of diacylglycerol acyltransferase 2 in a cell or tissue of ananimal. The method includes contacting the cell or tissue with acompound of the invention. Preferably, expression of diacylglycerolacyltransferase 2 is inhibited in the present method. Typically, thetissue of the animal is white adipose tissue or brown adipose tissue.

The compounds of the invention are further useful in methods formodulating fatty acid synthesis, lipogenesis, or gluconeogenesis, amongothers, in an animal. Typically, the animal is contacted with a compoundof the invention. The modulation of lipogenesis can be determined by achange in the mRNA level of a nucleic acid encoding a lipogenic gene.The lipogenic gene is selected from among glycerol kinase, ATP-citratelyase, acetyl-CoA carboxylase 1, acetyl-CoA carboxylase 2, fatty acidsynthase, carnitine palmitoyltransferase I, stearoyl-CoA desaturase,HMG-CoA reductase, lipoprotein lipase and sterol regulatory bindingelement protein 1.

The compounds of the invention are additionally useful for reducing theliver weight of an animal. For this use, the animal is contacted with acompound of the invention. Typically, the animal is obese or diabetic.

F. Modifications

As is known in the art, a nucleoside is a base-sugar combination. Thebase portion of the nucleoside is normally a heterocyclic base sometimesreferred to as a “nucleobase” or simply a “base”. The two most commonclasses of such heterocyclic bases are the purines and the pyrimidines.Nucleotides are nucleosides that further include a phosphate groupcovalently linked to the sugar portion of the nucleoside. For thosenucleosides that include a pentofuranosyl sugar, the phosphate group canbe linked to the 2′, 3′ or 5′ hydroxyl moiety of the sugar. In formingoligonucleotides, the phosphate groups covalently link adjacentnucleosides to one another to form a linear polymeric compound. In turn,the respective ends of this linear polymeric compound can be furtherjoined to form a circular compound, however, linear compounds aregenerally preferred. In addition, linear compounds may have internalnucleobase complementarity and may therefore fold in a manner as toproduce a fully or partially double-stranded compound. Withinoligonucleotides, the phosphate groups are commonly referred to asforming the internucleoside backbone of the oligonucleotide. The normallinkage or backbone of RNA and DNA is a 3′ to 5′ phosphodiester linkage.

Modified Internucleoside Linkages (Backbones)

Antisense compounds useful in this invention include oligonucleotidescontaining modified backbones or non-natural internucleoside linkages.As used herein, and “oligonucleotide mimetic” or “mimetic” refers to anycompound of the invention which is modified from the naturally occurringRNA or DNA nucleic acids. As defined herein, oligonucleotides havingmodified backbones include those that retain a phosphorus atom in thebackbone and those that do not have a phosphorus atom in the backbone.For the purposes of this specification, and as sometimes referenced inthe art, modified oligonucleotides that do not have a phosphorus atom intheir internucleoside backbone can also be considered to beoligonucleosides.

Preferred modified oligonucleotide backbones containing a phosphorusatom therein include, for example, phosphorothioates, chiralphosphorothioates, phosphorodithioates, phosphotriesters,aminoalkyl-phosphotriesters, methyl and other alkyl phosphonatesincluding 3′-alkylene phosphonates, 5′-alkylene phosphonates and chiralphosphonates, phosphinates, phosphoramidates including 3′-aminophosphoramidate and aminoalkylphosphoramidates, thionophosphoramidates,thionoalkylphosphonates, thionoalkylphosphotriesters, selenophosphatesand boranophosphates having normal 3′-5′ linkages, 2′-5′ linked analogsof these, and those having inverted polarity wherein one or moreinternucleotide linkages is a 3′ to 3′, 5′ to 5′ or 2′ to 2′ linkage.Preferred oligonucleotides having inverted polarity comprise a single 3′to 3′ linkage at the 3′-most internucleotide linkage i.e. a singleinverted nucleoside residue which may be abasic (the nucleobase ismissing or has a hydroxyl group in place thereof). Various salts, mixedsalts and free acid forms are also included.

Representative United States patents that teach the preparation of theabove phosphorus-containing linkages include, but are not limited to,U.S. Pat. Nos. 3,687,808; 4,469,863; 4,476,301; 5,023,243; 5,177,196;5,188,897; 5,264,423; 5,276,019; 5,278,302; 5,286,717; 5,321,131;5,399,676; 5,405,939; 5,453,496; 5,455,233; 5,466,677; 5,476,925;5,519,126; 5,536,821; 5,541,306; 5,550,111; 5,563,253; 5,571,799;5,587,361; 5,194,599; 5,565,555; 5,527,899; 5,721,218; 5,672,697 and5,625,050, each of which is herein incorporated by reference.

Preferred modified oligonucleotide backbones that do not include aphosphorus atom therein have backbones that are formed by short chainalkyl or cycloalkyl internucleoside linkages, mixed heteroatom and alkylor cycloalkyl internucleoside linkages, or one or more short chainheteroatomic or heterocyclic internucleoside linkages. These includethose having morpholino linkages (formed in part from the sugar portionof a nucleoside); siloxane backbones; sulfide, sulfoxide and sulfonebackbones; formacetyl and thioformacetyl backbones; methylene formacetyland thioformacetyl backbones; riboacetyl backbones; alkene containingbackbones; sulfamate backbones; methyleneimino and methylenehydrazinobackbones; sulfonate and sulfonamide backbones; amide backbones; andothers having mixed N, O, S and CH₂ component parts.

Representative United States patents that teach the preparation of theabove oligonucleosides include, but are not limited to, U.S. Pat. Nos.5,034,506; 5,166,315; 5,185,444; 5,214,134; 5,216,141; 5,235,033;5,264,562; 5,264,564; 5,405,938; 5,434,257; 5,466,677; 5,470,967;5,489,677; 5,541,307; 5,561,225; 5,596,086; 5,602,240; 5,610,289;5,602,240; 5,608,046; 5,610,289; 5,618,704; 5,623,070; 5,663,312;5,633,360; 5,677,437; 5,792,608; 5,646,269 and 5,677,439, each of whichis herein incorporated by reference.

Modified Sugar and Internucleoside Linkages-Mimetics

In other preferred antisense compounds, e.g., oligonucleotide mimetics,both the sugar and the internucleoside linkage (i.e. the backbone) ofthe nucleotide units are replaced with novel groups. The nucleobaseunits are maintained for hybridization with an appropriate targetnucleic acid. One such oligonucleotide mimetic that has been shown tohave excellent hybridization properties, is referred to as a peptidenucleic acid (PNA). In PNA compounds, the sugar-backbone of anoligonucleotide is replaced with an amide containing backbone, inparticular an aminoethylglycine backbone. The nucleobases are retainedand are bound directly or indirectly to aza nitrogen atoms of the amideportion of the backbone. Representative United States patents that teachthe preparation of PNA compounds include, but are not limited to, U.S.Pat. Nos. 5,539,082; 5,714,331; and 5,719,262, each of which is hereinincorporated by reference. Further teaching of PNA compounds can befound in Nielsen et al., Science, 1991, 254, 1497-1500.

In certain embodiments of the invention are oligonucleotides withphosphorothioate backbones and oligonucleosides with heteroatombackbones, and in particular—CH₂—NH—O—CH₂—, —CH₂—N(CH₃)—O—CH₂-[known asa methylene (methylimino) or MMI backbone], —CH₂—O—N(CH₃)—CH₂—,—CH₂—N(CH₃)—N(CH₃)—CH₂— and —O—N(CH₃)—CH₂—CH₂— [wherein the nativephosphodiester backbone is represented as —O—P—O—CH₂—] of the abovereferenced U.S. Pat. No. 5,489,677, and the amide backbones of the abovereferenced U.S. Pat. No. 5,602,240. Also included are oligonucleotideshaving morpholino backbone structures of the above-referenced U.S. Pat.No. 5,034,506.

Modified Sugars

Oligonucleotide mimetics may also contain one or more substituted sugarmoieties. As such these may comprise one of the following at the 2′position: OH; F; O—, S—, or N-alkyl; O—, S—, or N-alkenyl; O—, S- orN-alkynyl; or O-alkyl-O-alkyl, wherein the alkyl, alkenyl and alkynylmay be substituted or unsubstituted C₁ to C₁₀ alkyl or C₂ to C₁₀ alkenyland alkynyl. Particularly preferred are O[(CH₂)_(n)O]_(m)CH₃,O(CH₂)_(n)OCH₃, O(CH₂)_(n)NH₂, O(CH₂)_(n)CH₃, O(CH₂)_(n)ONH₂, andO(CH₂)_(n)ON[(CH₂)_(n)CH₃]₂, where n and m are from 1 to about 10. Otheroligonucleotide mimetics may comprise one of the following at the 2′position: C₁ to C₁₀ lower alkyl, substituted lower alkyl, alkenyl,alkynyl, alkaryl, aralkyl, O-alkaryl or O-aralkyl, SH, SCH₃, OCN, Cl,Br, CN, CF₃, OCF₃, SOCH₃, SO₂CH₃, ONO₂, NO₂, N₃, NH₂, heterocycloalkyl,heterocycloalkaryl, aminoalkylamino, polyalkylamino, substituted silyl,an RNA cleaving group, a reporter group, an intercalator, a group forimproving the pharmacokinetic properties of an oligonucleotide, or agroup for improving the pharmacodynamic properties of anoligonucleotide, and other substituents having similar properties. Onemodification includes 2′-methoxyethoxy (2′-O—CH₂CH₂OCH₃, also known as2′-O-(2-methoxyethyl) or 2′-O-methoxyethyl or 2′-MOE) (Martin et al.,Helv. Chim. Acta, 1995, 78, 486-504) i.e., an alkoxyalkoxy group. Afurther modification includes 2′-dimethylaminooxyethoxy, i.e., aO(CH₂)₂ON(CH₃)₂ group, also known as 2′-DMAOE, as described in exampleshereinbelow, and 2′-dimethylaminoethoxyethoxy (also known in the art as2′-O-dimethyl-amino-ethoxy-ethyl or 2′-DMAEOE), i.e.,2′-O—CH₂—O—CH₂—N(CH₃)₂, also described in examples hereinbelow.

Other modifications include 2′-methoxy (2′-O—CH₃), 2′-amino(2′—NH₂)₂′-aminopropoxy (2′-OCH₂CH₂CH₂NH₂), (2′-CH₂—CH═CH₂),(2′-O—CH₂—CH═CH₂) and 2′-fluoro (2′-F). The 2′-modification may be inthe arabino (up) position or ribo (down) position. One 2′-arabinomodification is 2′-F. Similar modifications may also be made at otherpositions on the oligonucleotide, particularly the 3′ position of thesugar on the 3′ terminal nucleotide or in 2′-5′ linked oligonucleotidesand the 5′ position of 5′ terminal nucleotide. Oligonucleotide mimeticsinvolving the sugar, such as cyclobutyl moieties in place of thepentofuranosyl sugar, are also within the scope of the presentinvention. Representative United States patents that teach thepreparation of such modified sugar structures include, but are notlimited to, U.S. Pat. Nos. 4,981,957; 5,118,800; 5,319,080; 5,359,044;5,393,878; 5,446,137; 5,466,786; 5,514,785; 5,519,134; 5,567,811;5,576,427; 5,591,722; 5,597,909; 5,610,300; 5,627,053; 5,639,873;5,646,265; 5,658,873; 5,670,633; 5,792,747; and 5,700,920, each of whichis herein incorporated by reference in its entirety.

A further modification of the sugar includes Locked Nucleic Acids (LNAs)in which the 2′-hydroxyl group is linked to the 3′ or 4′ carbon atom ofthe sugar ring, thereby forming a bicyclic sugar moiety. The linkage ispreferably a methylene (—CH₂—)_(n) group bridging the 2′ oxygen atom andthe 4′ carbon atom wherein n is 1 or 2. However, the present inventioncomprehends ethylene linkages as well. LNAs and preparation thereof aredescribed in International Patent Publication Nos. WO 98/39352 and WO99/14226.

Natural and Modified Nucleobases

Oligonucleotide mimetics also include nucleobase (often referred to inthe art as heterocyclic base or simply as “base”) modifications orsubstitutions. As used herein, “unmodified” or “natural” nucleobasesinclude the purine bases adenine (A) and guanine (G), and the pyrimidinebases thymine (T), cytosine (C) and uracil (U). Modified nucleobasesinclude other synthetic and natural nucleobases such as 5-methylcytosine(5-me-C), 5-hydroxymethyl cytosine, xanthine, hypoxanthine,2-aminoadenine, 6-methyl and other alkyl derivatives of adenine andguanine, 2-propyl and other alkyl derivatives of adenine and guanine,2-thiouracil, 2-thiothymine and 2-thiocytosine, 5-halouracil andcytosine, 5-propynyl (—C≡C—CH₃) uracil and cytosine and other alkynylderivatives of pyrimidine bases, 6-azo uracil, cytosine and thymine,5-uracil (pseudouracil), 4-thiouracil, 8-halo, 8-amino, 8-thiol,8-thioalkyl, 8-hydroxyl and other 8-substituted adenines and guanines,5-halo particularly 5-bromo, 5-trifluoromethyl and other 5-substituteduracils and cytosines, 7-methylguanine and 7-methyladenine, 2-F-adenine,2-amino-adenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and7-deazaadenine and 3-deazaguanine and 3-deazaadenine. Further modifiednucleobases include tricyclic pyrimidines such as phenoxazine cytidine(1H-pyrimido[5,4-b][1,4]benzoxazin-2(3H)-one), phenothiazine cytidine(1H-pyrimido[5,4-b][1,4]benzothiazin-2(3H)-one), G-clamps such as asubstituted phenoxazine cytidine (e.g.9-(2-aminoethoxy)-H-pyrimido[5,4-b][1,4]benzoxazin-2(3H)-one), carbazolecytidine (2H-pyrimido[4,5-b]indol-2-one), pyridoindole cytidine(H-pyrido[3′,′:4,5]pyrrolo[2,3-d]pyrimidin-2-one). Modified nucleobasesmay also include those in which the purine or pyrimidine base isreplaced with other heterocycles, for example 7-deaza-adenine,7-deazaguanosine, 2-aminopyridine and 2-pyridone. Further nucleobasesinclude those disclosed in U.S. Pat. No. 3,687,808, those disclosed inThe Concise Encyclopedia Of Polymer Science And Engineering, pages858-859, Kroschwitz, J. I., ed. John Wiley & Sons, 1990, those disclosedby Englisch et al., Angewandte Chemie, International Edition, 1991, 30,613, and those disclosed by Sanghvi, Y. S., Chapter 15, AntisenseResearch and Applications, pages 289-302, Crooke, S.T. and Lebleu, B.,ed., CRC Press, 1993. Certain of these nucleobases are particularlyuseful for increasing the binding affinity of the compounds of theinvention. These include 5-substituted pyrimidines, 6-azapyrimidines andN-2, N-6 and O-6 substituted purines, including 2-aminopropyladenine,5-propynyluracil and 5-propynylcytosine. 5-methylcytosine substitutionshave been shown to increase nucleic acid duplex stability by 0.6-1.2° C.and are presently preferred base substitutions, even more particularlywhen combined with 2′-O-methoxyethyl sugar modifications.

Representative United States patents that teach the preparation ofcertain of the above noted modified nucleobases as well as othermodified nucleobases include, but are not limited to, the above notedU.S. Pat. No. 3,687,808, as well as U.S. Pat. Nos. 4,845,205; 5,130,302;5,134,066; 5,175,273; 5,367,066; 5,432,272; 5,457,187; 5,459,255;5,484,908; 5,502,177; 5,525,711; 5,552,540; 5,587,469; 5,594,121,5,596,091; 5,614,617; 5,645,985; 5,830,653; 5,763,588; 6,005,096;5,681,941; and 5,570,692, each of which is herein incorporated byreference.

Conjugates

Another modification of the antisense compounds of the inventioninvolves chemically linking to the antisense compound one or moremoieties or conjugates which enhance the activity, cellular distributionor cellular uptake of the oligonucleotide. These moieties or conjugatescan include conjugate groups covalently bound to functional groups suchas primary or secondary hydroxyl groups. Conjugate groups of theinvention include intercalators, reporter molecules, polyamines,polyamides, polyethylene glycols, polyethers, groups that enhance thepharmacodynamic properties of oligomers, and groups that enhance thepharmacokinetic properties of oligomers. Typical conjugate groupsinclude cholesterol, lipids, phospholipids, biotin, phenazine, folate,phenanthridine, anthraquinone, acridine, fluoresceins, rhodamines,coumarins, and dyes. Groups that enhance the pharmacodynamic properties,in the context of this invention, include groups that improve uptake,enhance resistance to degradation, and/or strengthen sequence-specifichybridization with the target nucleic acid. Groups that enhance thepharmacokinetic properties, in the context of this invention, includegroups that improve uptake, distribution, metabolism or excretion of thecompounds of the present invention. Representative conjugate groups aredisclosed in International Patent Application No. PCT/US92/09196, filedOct. 23, 1992, and U.S. Pat. No. 6,287,860, the entire disclosures ofwhich are incorporated herein by reference. Conjugate moieties includebut are not limited to lipid moieties such as a cholesterol moiety,cholic acid, a thioether, e.g., hexyl-5-tritylthiol, a thiocholesterol,an aliphatic chain, e.g., dodecandiol or undecyl residues, aphospholipid, e.g., di-hexadecyl-rac-glycerol or triethylammonium1,2-di-O-hexadecyl-rac-glycero-3-H-phosphonate, a polyamine or apolyethylene glycol chain, or adamantane acetic acid, a palmityl moiety,or an octadecylamine or hexylamino-carbonyl-oxycholesterol moiety.

Antisense compounds of the invention may also be conjugated to drugsubstances, for example, aspirin, warfarin, phenylbutazone, ibuprofen,suprofen, fenbufen, ketoprofen, (S)-(+)-pranoprofen, carprofen,dansylsarcosine, 2,3,5-triiodobenzoic acid, flufenamic acid, folinicacid, a benzothiadiazide, chlorothiazide, a diazepine, indomethicin, abarbiturate, a cephalosporin, a sulfa drug, an antidiabetic, anantibacterial or an antibiotic. Oligonucleotide-drug conjugates andtheir preparation are described in U.S. Pat. No. 6,656,730 which isincorporated herein by reference in its entirety.

Representative United States patents that teach the preparation of sucholigonucleotide conjugates include, but are not limited to, U.S. Pat.Nos. 4,828,979; 4,948,882; 5,218,105; 5,525,465; 5,541,313; 5,545,730;5,552,538; 5,578,717, 5,580,731; 5,580,731; 5,591,584; 5,109,124;5,118,802; 5,138,045; 5,414,077; 5,486,603; 5,512,439; 5,578,718;5,608,046; 4,587,044; 4,605,735; 4,667,025; 4,762,779; 4,789,737;4,824,941; 4,835,263; 4,876,335; 4,904,582; 4,958,013; 5,082,830;5,112,963; 5,214,136; 5,082,830; 5,112,963; 5,214,136; 5,245,022;5,254,469; 5,258,506; 5,262,536; 5,272,250; 5,292,873; 5,317,098;5,371,241, 5,391,723; 5,416,203, 5,451,463; 5,510,475; 5,512,667;5,514,785; 5,565,552; 5,567,810; 5,574,142; 5,585,481; 5,587,371;5,595,726; 5,597,696; 5,599,923; 5,599,928 and 5,688,941, each of whichis herein incorporated by reference.

Oligomeric compounds used in the compositions of the present inventioncan also be modified to have one or more stabilizing groups that aregenerally attached to one or both termini of oligomeric compounds toenhance properties such as for example nuclease stability. Included instabilizing groups are cap structures. By “cap structure or terminal capmoiety” is meant chemical modifications, which have been incorporated ateither terminus of oligonucleotides (see for example Wincott et al. andInternational Patent Publication No. WO 97/26270, incorporated byreference herein). These terminal modifications protect the oligomericcompounds having terminal nucleic acid molecules from exonucleasedegradation, and can help in delivery and/or localization within a cell.The cap can be present at the 5′-terminus (5′-cap) or at the 3′-terminus(3′-cap) or at both termini. In non-limiting examples, the 5′-capincludes inverted abasic residue (moiety), 4′,5′-methylene nucleotide;1-(beta-D-erythrofuranosyl) nucleotide, 4′-thio nucleotide, carbocyclicnucleotide; 1,5-anhydrohexitol nucleotide; L-nucleotides;alpha-nucleotides; modified base nucleotide; phosphorodithioate linkage;threo-pentofuranosyl nucleotide; acyclic 3′,4′-seco nucleotide; acyclic3,4-dihydroxybutyl nucleotide; acyclic 3,5-dihydroxypentylribonucleotide, 3′-3′-inverted nucleotide moiety; 3′-3′-inverted abasicmoiety; 3′-2′-inverted nucleotide moiety; 3′-2′-inverted abasic moiety;1,4-butanediol phosphate; 3′-phosphoramidate; hexylphosphate; aminohexylphosphate; 3′-phosphate; 3′-phosphorothioate; phosphorodithioate; orbridging or non-bridging methylphosphonate moiety (for more details seeWincott et al., International Patent Publication No. WO 97/26270,incorporated by reference herein).

Particularly preferred 3′-cap structures of the present inventioninclude, for example 4′,5′-methylene nucleotide;1-(beta-D-erythrofuranosyl) nucleotide; 4′-thio nucleotide, carbocyclicnucleotide; 5′-amino-alkyl phosphate; 1,3-diamino-2-propyl phosphate,3-aminopropyl phosphate; 6-aminohexyl phosphate; 1,2-aminododecylphosphate; hydroxypropyl phosphate; 1,5-anhydrohexitol nucleotide;L-nucleotide; alpha-nucleotide; modified base nucleotide;phosphorodithioate; threo-pentofuranosyl nucleotide; acyclic 3′,4′-seconucleotide; 3,4-dihydroxybutyl nucleotide; 3,5-dihydroxypentylnucleotide, 5′-5′-inverted nucleotide moiety; 5′-5′-inverted abasicmoiety; 5′-phosphoramidate; 5′-phosphorothioate; 1,4-butanediolphosphate; 5′-amino; bridging and/or non-bridging 5′-phosphoramidate,phosphorothioate and/or phosphorodithioate, bridging or non bridgingmethylphosphonate and 5′-mercapto moieties (for more details seeBeaucage and Tyer, 1993, Tetrahedron 49, 1925; incorporated by referenceherein).

Further 3′ and 5′-stabilizing groups that can be used to cap one or bothends of an oligomeric compound to impart nuclease stability includethose disclosed in International Patent Publication No. WO 03/004602,published Jan. 16, 2003.

Chimeric Compounds

It is not necessary for all positions in a given compound oroligonucleotide mimetic to be uniformly modified, and in fact one ormore of the aforementioned modifications may be incorporated in a singlecompound or even at a single nucleoside within an oligonucleotide.

The present invention also includes antisense compounds or mimeticswhich are chimeric compounds. “Chimeric” antisense compounds or“chimeras,” in the context of this invention, are antisense compounds,particularly oligonucleotides, which contain at least two chemicallydistinct regions, each made up of at least one monomer unit, i.e., anucleotide in the case of an oligonucleotide compound. Chimericantisense oligonucleotides are thus a form of antisense compound. Theseoligonucleotides typically contain at least one chemically distinctregion wherein the oligonucleotide is modified so as to confer upon theoligonucleotide increased resistance to nuclease degradation, increasedcellular uptake, increased stability and/or increased binding affinityfor the target nucleic acid. An additional chemically distinct region ofthe oligonucleotide may serve as a substrate for enzymes capable ofcleaving RNA:DNA or RNA:RNA hybrids. By way of example, RNase H is acellular endonuclease which cleaves the RNA strand of an RNA:DNA duplex.Modifications that activate, recruit or trigger RNase H and result incleavage of the RNA target thereby greatly enhance the efficiency ofoligonucleotide-mediated inhibition of gene expression. The cleavage ofRNA:RNA hybrids can, in like fashion, be accomplished through theactions of endoribonucleases such as RnaseL, which cleaves both cellularand viral RNA. Cleavage of the RNA target can be routinely detected bygel electrophoresis and, if necessary, associated nucleic acidhybridization techniques known in the art.

Preferred chimeric oligonucleotides are those disclosed in the Examplesherein. Particularly preferred chimeric oligonucleotides are thosereferred to as SEQ ID NOS: 65, 26, 29, and 35, as well as those chimericoligonucleotides set forth in Tables 2, 3, 14, and 15 and specified inthe Examples below. Preferred siRNAs are those referred to as SEQ IDNos: 238, 242, 243, 251, and 252, as well as those set forth in Table 11and specified in the Examples below. Chimeric antisense compounds of theinvention may be formed as composite structures of two or moreoligonucleotides, modified oligonucleotides, oligonucleosides and/oroligonucleotide mimetics as described above. Chimeric antisensecompounds can be of several different types. These include a first typewherein the “gap” segment of linked nucleosides is positioned between 5′and 3′ “wing” segments of linked nucleosides and a second “open end”type wherein the “gap” segment is located at either the 3′ or the 5′terminus of the chimeric antisense compound. Compounds of the first typeare also known in the art as “gapmers” or gapped oligonucleotides.Compounds of the second type are also known in the art as “hemimers” or“wingmers”. Such compounds have also been referred to in the art ashybrids. In a gapmer that is 20 nucleotides in length, a gap or wing canbe 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17 or 18nucleotides in length. In one embodiment, a 20-nucleotide gapmer iscomprised of a gap 8 nucleotides in length, flanked on both the 5′ and3′ sides by wings 6 nucleotides in length. In another embodiment, a20-nucleotide gapmer is comprised of a gap 10 nucleotides in length,flanked on both the 5′ and 3′ sides by wings 5 nucleotides in length. Inanother embodiment, a 20-nucleotide gapmer is comprised of a gap 12nucleotides in length flanked on both the 5′ and 3′ sides by wings 4nucleotides in length. In a further embodiment, a 20-nucleotide gapmeris comprised of a gap 14 nucleotides in length flanked on both the 5′and 3′ sides by wings 3 nucleotides in length. In another embodiment, a20-nucleotide gapmer is comprised of a gap 16 nucleotides in lengthflanked on both the 5′ and 3′ sides by wings 2 nucleotides in length. Ina further embodiment, a 20-nucleotide gapmer is comprised of a gap 18nucleotides in length flanked on both the 5′ and 3′ ends by wings 1nucleotide in length. Alternatively, the wings are of different lengths,for example, a 20-nucleotide gapmer may be comprised of a gap 10nucleotides in length, flanked by a 6-nucleotide wing on one side (5′ or3′) and a 4-nucleotide wing on the other side (5′ or 3′).

In a hemimer, an “open end” chimeric antisense compound having twochemically distinct regions, a first chemically distinct region, or thegap segment, in a compound 20 nucleotides in length can be located ateither the 5′ or 3′ terminus of the oligomeric compound, can be 1, 2, 3,4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18 or 19 nucleotidesin length. A second chemically distinct region in a compound 20nucleotides in length can be located at the 3′ terminus of the compoundand can be 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18or 19 nucleotides in length. For example, a 20-nucleotide hemimer canhave a first chemically distinct region, or a gap segment, of 10nucleotides at the 5′ end and a second segment of 10 nucleotides at the3′ end.

Representative United States patents that teach the preparation of suchhybrid structures include, but are not limited to, U.S. Pat. Nos.5,013,830; 5,149,797; 5,220,007; 5,256,775; 5,366,878; 5,403,711;5,491,133; 5,565,350; 5,623,065; 5,652,355; 5,652,356; and 5,700,922,each of which is herein incorporated by reference in its entirety.

G. Formulations

The compounds of the invention may also be admixed, encapsulated,conjugated or otherwise associated with other molecules, moleculestructures or mixtures of compounds, as for example, liposomes,receptor-targeted molecules, oral, rectal, topical or otherformulations, for assisting in uptake, distribution and/or absorption.Representative United States patents that teach the preparation of suchuptake, distribution and/or absorption-assisting formulations include,but are not limited to, U.S. Pat. Nos. 5,108,921; 5,354,844; 5,416,016;5,459,127; 5,521,291; 5,543,158; 5,547,932; 5,583,020; 5,591,721;4,426,330; 4,534,899; 5,013,556; 5,108,921; 5,213,804; 5,227,170;5,264,221; 5,356,633; 5,395,619; 5,416,016; 5,417,978; 5,462,854;5,469,854; 5,512,295; 5,527,528; 5,534,259; 5,543,152; 5,556,948;5,580,575; and 5,595,756, each of which is herein incorporated byreference.

The antisense compounds of the invention encompass any pharmaceuticallyacceptable salts, esters, or salts of such esters, or any other compoundwhich, upon administration to an animal, including a human, is capableof providing (directly or indirectly) the biologically active metaboliteor residue thereof. Accordingly, for example, the disclosure is alsodrawn to prodrugs and pharmaceutically acceptable salts of the compoundsof the invention, pharmaceutically acceptable salts of such prodrugs,and other bioequivalents.

The term “prodrug” indicates a therapeutic agent that is prepared in aninactive form that is converted to an active form (i.e., drug) withinthe body or cells thereof by the action of endogenous enzymes or otherchemicals and/or conditions. In particular, prodrug versions of theoligonucleotides of the invention are prepared as SATE[(S-acetyl-2-thioethyl) phosphate] derivatives according to the methodsdisclosed in International Patent Publication No. WO 93/24510 toGosselin et al., published Dec. 9, 1993 or in International PatentPublication No. WO 94/26764 and U.S. Pat. No. 5,770,713 to Imbach et al.

The term “pharmaceutically acceptable salts” refers to physiologicallyand pharmaceutically acceptable salts of the compounds of the invention:i.e., salts that retain the desired biological activity of the parentcompound and do not impart undesired toxicological effects thereto. Foroligonucleotides, preferred examples of pharmaceutically acceptablesalts and their uses are further described in U.S. Pat. No. 6,287,860,which is incorporated herein in its entirety.

Pharmaceutically acceptable base addition salts are formed with metalsor amines, such as alkali and alkaline earth metals or organic amines.Examples of metals used as cations are sodium, potassium, magnesium,calcium, and the like. Examples of suitable amines areN,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine,dicyclohexylamine, ethylenediamine, N-methylglucamine, and procaine(see, for example, Berge et al., “Pharmaceutical Salts,” J. of PharmaSci., 1977, 66, 1-19). The base addition salts of said acidic compoundsare prepared by contacting the free acid form with a sufficient amountof the desired base to produce the salt in the conventional manner. Thefree acid form may be regenerated by contacting the salt form with anacid and isolating the free acid in the conventional manner. The freeacid forms differ from their respective salt forms somewhat in certainphysical properties such as solubility in polar solvents, but otherwisethe salts are equivalent to their respective free acid for purposes ofthe present invention. As used herein, a “pharmaceutical addition salt”includes a pharmaceutically acceptable salt of an acid form of one ofthe components of the compositions of the invention. These includeorganic or inorganic acid salts of the amines. Preferred acid salts arethe hydrochlorides, acetates, salicylates, nitrates and phosphates.Other suitable pharmaceutically acceptable salts are well known to thoseskilled in the art and include basic salts of a variety of inorganic andorganic acids, such as, for example, with inorganic acids, such as forexample hydrochloric acid, hydrobromic acid, sulfuric acid or phosphoricacid; with organic carboxylic, sulfonic, sulfo or phospho acids orN-substituted sulfamic acids, for example acetic acid, propionic acid,glycolic acid, succinic acid, maleic acid, hydroxymaleic acid,methylmaleic acid, fumaric acid, malic acid, tartaric acid, lactic acid,oxalic acid, gluconic acid, glucaric acid, glucuronic acid, citric acid,benzoic acid, cinnamic acid, mandelic acid, salicylic acid,4-aminosalicylic acid, 2-phenoxybenzoic acid, 2-acetoxybenzoic acid,embonic acid, nicotinic acid or isonicotinic acid; and with amino acids,such as the 20 alpha-amino acids involved in the synthesis of proteinsin nature, for example glutamic acid or aspartic acid, and also withphenylacetic acid, methanesulfonic acid, ethanesulfonic acid,2-hydroxyethanesulfonic acid, ethane-1,2-disulfonic acid,benzenesulfonic acid, 4-methylbenzenesulfonic acid,naphthalene-2-sulfonic acid, naphthalene-1,5-disulfonic acid, 2- or3-phosphoglycerate, glucose-6-phosphate, N-cyclohexylsulfamic acid (withthe formation of cyclamates), or with other acid organic compounds, suchas ascorbic acid. Pharmaceutically acceptable salts of compounds mayalso be prepared with a pharmaceutically acceptable cation. Suitablepharmaceutically acceptable cations are well known to those skilled inthe art and include alkaline, alkaline earth, ammonium and quaternaryammonium cations. Carbonates or hydrogen carbonates are also possible.

For oligonucleotides, preferred examples of pharmaceutically acceptablesalts include but are not limited to (a) salts formed with cations suchas sodium, potassium, ammonium, magnesium, calcium, polyamines such asspermine and spermidine, etc.; (b) acid addition salts formed withinorganic acids, for example hydrochloric acid, hydrobromic acid,sulfuric acid, phosphoric acid, nitric acid and the like; (c) saltsformed with organic acids such as, for example, acetic acid, oxalicacid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconicacid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid,palmitic acid, alginic acid, polyglutamic acid, naphthalenesulfonicacid, methanesulfonic acid, p-toluenesulfonic acid,naphthalenedisulfonic acid, polygalacturonic acid, and the like; and (d)salts formed from elemental anions such as chlorine, bromine, andiodine.

The present invention also includes pharmaceutical compositions andformulations which include the antisense compounds of the invention. Thepharmaceutical compositions of the present invention may be administeredin a number of ways depending upon whether local or systemic treatmentis desired and upon the area to be treated. Administration may betopical (including ophthalmic and to mucous membranes including vaginaland rectal delivery), pulmonary, e.g., by inhalation or insufflation ofpowders or aerosols, including by nebulizer; intratracheal, intranasal,epidermal and transdermal), oral or parenteral. Parenteraladministration includes intravenous, intraarterial, subcutaneous,intraperitoneal or intramuscular injection or infusion; or intracranial,e.g., intrathecal or intraventricular, administration. Oligonucleotideswith at least one 2′-O-methoxyethyl modification are believed to beparticularly useful for oral administration.

Pharmaceutical compositions and formulations for topical administrationmay include transdermal patches, ointments, lotions, creams, gels,drops, suppositories, sprays, liquids and powders. Conventionalpharmaceutical carriers, aqueous, powder or oily bases, thickeners andthe like may be necessary or desirable. Coated condoms, gloves and thelike may also be useful.

Preferred topical formulations include those in which theoligonucleotides of the invention are in admixture with a topicaldelivery agent such as lipids, liposomes, fatty acids, fatty acidesters, steroids, chelating agents and surfactants. Preferred lipids andliposomes include neutral (e.g. dioleoylphosphatidyl DOPE ethanolamine,dimyristoylphosphatidyl choline DMPC, distearolyphosphatidyl choline)negative (e.g. dimyristoylphosphatidyl glycerol DMPG) and cationic (e.g.dioleoyltetramethylaminopropyl DOTAP and dioleoylphosphatidylethanolamine DOTMA). Oligonucleotides of the invention may beencapsulated within liposomes or may form complexes thereto, inparticular to cationic liposomes. Alternatively, oligonucleotides may becomplexed to lipids, in particular to cationic lipids. Preferred fattyacids and esters include but are not limited arachidonic acid, oleicacid, eicosanoic acid, lauric acid, caprylic acid, capric acid, myristicacid, palmitic acid, stearic acid, linoleic acid, linolenic acid,dicaprate, tricaprate, monoolein, dilaurin, glyceryl 1-monocaprate,1-dodecylazacycloheptan-2-one, an acylcarnitine, an acylcholine, or aC₁₋₁₀ alkyl ester (e.g. isopropylmyristate IPM), monoglyceride,diglyceride or pharmaceutically acceptable salt thereof. Topicalformulations are described in detail in U.S. Pat. No. 6,747,014, whichis incorporated herein by reference in its entirety.

In some embodiments, an oligonucleotide may be administered to a subjectvia an oral route of administration. The subjects of the presentinvention comprise animals. An animal subject may be a mammal, such as amouse, a rat, a dog, a guinea pig, a human, a non-human primate, a cator a pig. Non-human primates include monkeys and chimpanzees. A suitableanimal subject may be an experimental animal, such as a mouse, a rat, adog, a non-human primate, a cat or a pig.

In some embodiments, the subject may be a human. In certain embodiments,the subject may be a human patient as discussed in more detail herein.In certain embodiments, it may be necessary to modulate the expressionof one or more genes of the human patient. In some particularembodiments, it may be necessary to inhibit expression of one or moregenes of the human patient. In particular embodiments, it may benecessary to modulate, i.e. inhibit or enhance, diacylglycerolacyltransferase 2 in order to obtain therapeutic outcomes discussedherein.

In some embodiments, non-parenteral (e.g. oral) oligonucleotideformulations according to the present invention result in enhancedbioavailability of the oligonucleotide. In this context, the term“bioavailability” refers to a measurement of that portion of anadministered drug which reaches the circulatory system (e.g. blood,especially blood plasma) when a particular mode of administration isused to deliver the drug Enhanced bioavailability refers to a particularmode of administration's ability to deliver oligonucleotide to theperipheral blood plasma of a subject relative to another mode ofadministration. For example, when a non-parenteral mode ofadministration (e.g. an oral mode) is used to introduce the drug into asubject, the bioavailability for that mode of administration may becompared to a different mode of administration, e.g. an IV mode ofadministration. In some embodiments, the area under a compound's bloodplasma concentration curve (AUC₀) after non-parenteral administrationmay be divided by the area under the drug's plasma concentration curveafter intravenous (i.v.) administration (AUC_(iv)) to provide adimensionless quotient (relative bioavailability, RB) that representsfraction of compound absorbed via the non-parenteral route as comparedto the IV route. A composition's bioavailability is said to be enhancedin comparison to another composition's bioavailability when the firstcomposition's relative bioavailability (RB₁) is greater than the secondcomposition's relative bioavailability (RB₂).

In general, bioavailability correlates with therapeutic efficacy when acompound's therapeutic efficacy is related to the blood concentrationachieved, even if the drug's ultimate site of action is intracellular(van Berge-Henegouwen et al., Gastroenterol., 1977, 73, 300).Bioavailability studies have been used to determine the degree ofintestinal absorption of a drug by measuring the change in peripheralblood levels of the drug after an oral dose (DiSanto, Chapter 76 In:Remington's Pharmaceutical Sciences, 18th Ed., Gennaro, ed., MackPublishing Co., Easton, Pa., 1990, pages 1451-1458).

In general, the bioavailability of an oral composition (comprising anoligonucleotide) is said to be “enhanced” when its relativebioavailability is greater than the bioavailability of a compositionsubstantially consisting of pure oligonucleotide, i.e. oligonucleotidein the absence of a penetration enhancer.

Organ bioavailability refers to the concentration of compound in anorgan. Organ bioavailability may be measured in test subjects by anumber of means, such as by whole-body radiography. Organbioavailability may be modified, e.g. enhanced, by one or moremodifications to the oligonucleotide, by use of one or more carriercompounds or excipients, etc. as discussed in more detail herein. Ingeneral, an increase in bioavailability will result in an increase inorgan bioavailability.

Oral oligonucleotide compositions according to the present invention maycomprise one or more “mucosal penetration enhancers,” also known as“absorption enhancers” or simply as “penetration enhancers.”Accordingly, some embodiments of the invention comprise at least oneoligonucleotide in combination with at least one penetration enhancer.In general, a penetration enhancer is a substance that facilitates thetransport of a drug across mucous membrane(s) associated with thedesired mode of administration, e.g. intestinal epithelial membranes.Accordingly it is desirable to select one or more penetration enhancersthat facilitate the uptake of an oligonucleotide, without interferingwith the activity of the oligonucleotide, and in such a manner theoligonucleotide can be introduced into the body of an animal withoutunacceptable degrees of side-effects such as toxicity, irritation orallergic response.

Embodiments of the present invention provide compositions comprising oneor more pharmaceutically acceptable penetration enhancers, and methodsof using such compositions, which result in the improved bioavailabilityof oligonucleotides administered via non-parenteral modes ofadministration. Heretofore, certain penetration enhancers have been usedto improve the bioavailability of certain drugs. See Muranishi, Crit.Rev. Ther. Drug Carrier Systems, 1990, 7, 1 and Lee et al., Crit. Rev.Ther. Drug Carrier Systems, 1991, 8, 91. It has been found that theuptake and delivery of oligonucleotides can be greatly improved evenwhen administered by non-parenteral means through the use of a number ofdifferent classes of penetration enhancers.

In some embodiments, compositions for non-parenteral administrationinclude one or more modifications to naturally-occurringoligonucleotides (i.e. full-phosphodiester deoxyribosyl orfull-phosphodiester ribosyl oligonucleotides). Such modifications mayincrease binding affinity, nuclease stability, cell or tissuepermeability, tissue distribution, or other biological orpharmacokinetic property. Modifications may be made to the base, thelinker, or the sugar, in general, as discussed in more detail hereinwith regards to oligonucleotide chemistry. In some embodiments of theinvention, compositions for administration to a subject, and inparticular oral compositions for administration to an animal (human ornon-human) subject, will comprise modified oligonucleotides having oneor more modifications for enhancing affinity, stability, tissuedistribution, or other biological property.

Suitable modified linkers include phosphorothioate linkers. In someembodiments according to the invention, the oligonucleotide has at leastone phosphorothioate linker. Phosphorothioate linkers provide nucleasestability as well as plasma protein binding characteristics to theoligonucleotide. Nuclease stability is useful for increasing the in vivolifetime of oligonucleotides, while plasma protein binding decreases therate of first pass clearance of oligonucleotide via renal excretion. Insome embodiments according to the present invention, the oligonucleotidehas at least two phosphorothioate linkers. In some embodiments, whereinthe oligonucleotide has exactly n nucleosides, the oligonucleotide hasfrom one to n−1 phosphorothioate linkages. In some embodiments, whereinthe oligonucleotide has exactly n nucleosides, the oligonucleotide hasn−1 phosphorothioate linkages. In other embodiments wherein theoligonucleotide has exactly n nucleoside, and n is even, theoligonucleotide has from 1 to n/2 phosphorothioate linkages, or, when nis odd, from 1 to (n−1)/2 phosphorothioate linkages. In someembodiments, the oligonucleotide has alternating phosphodiester (PO) andphosphorothioate (PS) linkages. In other embodiments, theoligonucleotide has at least one stretch of two or more consecutive POlinkages and at least one stretch of two or more PS linkages. In otherembodiments, the oligonucleotide has at least two stretches of POlinkages interrupted by at least one PS linkage.

In some embodiments, at least one of the nucleosides is modified on theribosyl sugar unit by a modification that imparts nuclease stability,binding affinity or some other beneficial biological property to thesugar. In some cases, the sugar modification includes a 2′-modification,e.g. the 2′-OH of the ribosyl sugar is replaced or substituted. Suitablereplacements for 2′-OH include 2′-F and 2′-arabino-F. Suitablesubstitutions for OH include 2′-O-alkyl, e.g. 2-O-methyl, and2′-O-substituted alkyl, e.g. 2′-O-methoxyethyl, 2′-NH₂,2′-O-aminopropyl, etc. In some embodiments, the oligonucleotide containsat least one 2′-modification. In some embodiments, the oligonucleotidecontains at least two 2′-modifications. In some embodiments, theoligonucleotide has at least one 2′-modification at each of the termini(i.e. the 3′-and 5′-terminal nucleosides each have the same or different2′-modifications). In some embodiments, the oligonucleotide has at leasttwo sequential 2′-modifications at each end of the oligonucleotide. Insome embodiments, oligonucleotides further comprise at least onedeoxynucleoside. In particular embodiments, oligonucleotides comprise astretch of deoxynucleosides such that the stretch is capable ofactivating RNase (e.g. RNase H) cleavage of an RNA to which theoligonucleotide is capable of hybridizing. In some embodiments, astretch of deoxynucleosides capable of activating RNase-mediatedcleavage of RNA comprises about 6 to about 16, e.g. about 8 to about 16consecutive deoxynucleosides. In further embodiments, oligonucleotidesare capable of eliciting cleaveage by dsRNAse enzymes which act onRNA:RNA hybrids.

Oligonucleotide compositions of the present invention may be formulatedin various dosage forms such as, but not limited to, tablets, capsules,liquid syrups, soft gels, suppositories, and enemas. The term“alimentary delivery” encompasses e.g. oral, rectal, endoscopic andsublingual/buccal administration. A common requirement for these modesof administration is absorption over some portion or all of thealimentary tract and a need for efficient mucosal penetration of theoligonucleotides or mimetics thereof so administered.

Delivery of a drug via the oral mucosa, as in the case of buccal andsublingual administration, has several desirable features, including, inmany instances, a more rapid rise in plasma concentration of the drug(Harvey, Chapter 35 In: Remington's Pharmaceutical Sciences, 18th Ed.,Gennaro, ed., Mack Publishing Co., Easton, Pa., 1990, page 711).

Endoscopy may be used for drug delivery directly to an interior portionof the alimentary tract. For example, endoscopic retrogradecystopancreatography (ERCP) takes advantage of extended gastroscopy andpermits selective access to the biliary tract and the pancreatic duct(Hirahata et al., Gan To Kagaku Ryoho, 1992, 19(10 Suppl.), 1591).Pharmaceutical compositions, including liposomal formulations, can bedelivered directly into portions of the alimentary canal, such as, e.g.,the duodenum (Somogyi et al., Pharm. Res., 1995, 12, 149) or the gastricsubmucosa (Akamo et al., Japanese J. Cancer Res., 1994, 85, 652) viaendoscopic means. Gastric lavage devices (Inoue et al., Artif. Organs,1997, 21, 28) and percutaneous endoscopic feeding devices (Pennington etal., Ailment Pharmacol. Ther., 1995, 9, 471) can also be used for directalimentary delivery of pharmaceutical compositions.

In some embodiments, oligonucleotide formulations may be administeredthrough the anus into the rectum or lower intestine. Rectalsuppositories, retention enemas or rectal catheters can be used for thispurpose and may be preferred when patient compliance might otherwise bedifficult to achieve (e.g., in pediatric and geriatric applications, orwhen the patient is vomiting or unconscious). Rectal administration canresult in more prompt and higher blood levels than the oral route.(Harvey, Chapter 35 In: Remington's Pharmaceutical Sciences, 18th Ed.,Gennaro, ed., Mack Publishing Co., Easton, Pa., 1990, page 711). Becauseabout 50% of the drug that is absorbed from the rectum will likelybypass the liver, administration by this route significantly reduces thepotential for first-pass metabolism (Benet et al., Chapter 1 In: Goodman& Gilman's The Pharmacological Basis of Therapeutics, 9th Ed., Hardmanet al., eds., McGraw-Hill, New York, N.Y., 1996).

Some embodiments employ various penetration enhancers in order to effecttransport of oligonucleotides and other nucleic acids across mucosal andepithelial membranes. Penetration enhancers may be classified asbelonging to one of five broad categories—surfactants, fatty acids, bilesalts, chelating agents, and non-chelating non-surfactants (Lee et al.,Critical Reviews in Therapeutic Drug Carrier Systems, 1991, p. 92).Accordingly, some embodiments comprise oral oligonucleotide compositionscomprising at least one member of the group consisting of surfactants,fatty acids, bile salts, chelating agents, and non-chelatingsurfactants. Further embodiments comprise oral oligonucleotidecompositions comprising at least one fatty acid, e.g. capric or lauricacid, or combinations or salts thereof. Other embodiments comprisemethods of enhancing the oral bioavailability of an oligonucleotide, themethod comprising co-administering the oligonucleotide and at least onepenetration enhancer.

Other excipients that may be added to oral oligonucleotide compositionsinclude surfactants (or “surface-active agents”). These are chemicalentities which, when dissolved in an aqueous solution, reduce thesurface tension of the solution or the interfacial tension between theaqueous solution and another liquid, with the result that absorption ofoligonucleotides through the alimentary mucosa and other epithelialmembranes is enhanced. In addition to bile salts and fatty acids,surfactants include, for example, sodium lauryl sulfate,polyoxyethylene-9-lauryl ether and polyoxyethylene-20-cetyl ether (Leeet al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, page92); and perfluorohemical emulsions, such as FC-43 (Takahashi et al., J.Pharm. Phamacol., 1988, 40, 252).

Fatty acids and their derivatives which act as penetration enhancers andmay be used in compositions of the present invention include, forexample, oleic acid, lauric acid, capric acid (n-decanoic acid),myristic acid, palmitic acid, stearic acid, linoleic acid, linolenicacid, dicaprate, tricaprate, monoolein (1-monooleoyl-rac-glycerol),dilaurin, caprylic acid, arachidonic acid, glyceryl 1-monocaprate,1-dodecylazacycloheptan-2-one, acylcarnitines, acylcholines and mono-and di-glycerides thereof and/or physiologically acceptable saltsthereof (i.e., oleate, laurate, caprate, myristate, palmitate, stearate,linoleate, etc.) (Lee et al., Critical Reviews in Therapeutic DrugCarrier Systems, 1991, page 92; Muranishi, Critical Reviews inTherapeutic Drug Carrier Systems, 1990, 7, 1; El-Hariri et al., J.Pharm. Pharmacol., 1992, 44, 651).

A variety of bile salts also function as penetration enhancers tofacilitate the uptake and bioavailability of drugs. The physiologicalroles of bile include the facilitation of dispersion and absorption oflipids and fat-soluble vitamins (Brunton, Chapter 38 In: Goodman &Gilman's The Pharmacological Basis of Therapeutics, 9th Ed., Hardman etal., eds., McGraw-Hill, New York, N.Y., 1996, pages 934-935). Variousnatural bile salts, and their synthetic derivatives, act as penetrationenhancers. Thus, the term “bile salt” includes any of the naturallyoccurring components of bile as well as any of their syntheticderivatives. The bile salts of the invention include, for example,cholic acid (or its pharmaceutically acceptable sodium salt, sodiumcholate), dehydrocholic acid (sodium dehydrocholate), deoxycholic acid(sodium deoxycholate), glucholic acid (sodium glucholate), glycholicacid (sodium glycocholate), glycodeoxycholic acid (sodiumglycodeoxycholate), taurocholic acid (sodium taurocholate),taurodeoxycholic acid (sodium taurodeoxycholate), chenodeoxycholic acid(CDCA, sodium chenodeoxycholate), ursodeoxycholic acid (UDCA), sodiumtauro-24,25-dihydro-fusidate (STDHF), sodium glycodihydrofusidate andpolyoxyethylene-9-lauryl ether (POE) (Lee et al., Critical Reviews inTherapeutic Drug Carrier Systems, 1991, page 92; Swinyard, Chapter 39In: Remington's Pharmaceutical Sciences, 18th Ed., Gennaro, ed., MackPublishing Co., Easton, Pa., 1990, pages 782-783; Muranishi, CriticalReviews in Therapeutic Drug Carrier Systems, 1990, 7, 1; Yamamoto etal., J. Pharm. Exp. Ther., 1992, 263, 25; Yamashita et al., J. Pharm.Sci., 1990, 79, 579).

In some embodiments, penetration enhancers of the present invention aremixtures of penetration enhancing compounds. One such penetrationmixture is UDCA (and/or CDCA) with capric and/or lauric acids or saltsthereof e.g. sodium. Such mixtures are useful for enhancing the deliveryof biologically active substances across mucosal membranes, inparticular intestinal mucosa. Other penetration enhancer mixturescomprise about 5-95% of bile acid or salt(s) UDCA and/or CDCA with 5-95%capric and/or lauric acid. Particular penetration enhancers are mixturesof the sodium salts of UDCA, capric acid and lauric acid in a ratio ofabout 1:2:2 respectively. Another such penetration enhancer is a mixtureof capric and lauric acid (or salts thereof) in a 0.01:1 to 1:0.01 ratio(mole basis). In particular embodiments capric acid and lauric acid arepresent in molar ratios of e.g. about 0.1:1 to about 1:0.1, inparticular about 0.5:1 to about 1:0.5.

Other excipients include chelating agents, i.e. compounds that removemetallic ions from solution by forming complexes therewith, with theresult that absorption of oligonucleotides through the alimentary andother mucosa is enhanced. With regards to their use as penetrationenhancers in compositions containing DNA-like oligonucleotides of thepresent invention, chelating agents have the added advantage of alsoserving as DNase inhibitors, as most characterized DNA nucleases requirea divalent metal ion for catalysis and are thus inhibited by chelatingagents (Jarrett, J. Chromatogr., 1993, 618, 315). Chelating agents ofthe invention include, but are not limited to, disodiumethylenediaminetetraacetate (EDTA), citric acid, salicylates (e.g.,sodium salicylate, 5-methoxysalicylate and homovanilate), N-acylderivatives of collagen, laureth-9 and N-amino acyl derivatives ofbeta-diketones (enamines)(Lee et al., Critical Reviews in TherapeuticDrug Carrier Systems, 1991, page 92; Muranishi, Critical Reviews inTherapeutic Drug Carrier Systems, 1990, 7, 1; Buur et al., J. ControlRel., 1990, 14, 43).

As used herein, non-chelating non-surfactant penetration enhancers maybe defined as compounds that demonstrate insignificant activity aschelating agents or as surfactants but that nonetheless enhanceabsorption of oligonucleotides through the alimentary and other mucosalmembranes (Muranishi, Critical Reviews in Therapeutic Drug CarrierSystems, 1990, 7, 1). This class of penetration enhancers includes, butis not limited to, unsaturated cyclic ureas, 1-alkyl- and1-alkenylazacyclo-alkanone derivatives (Lee et al., Critical Reviews inTherapeutic Drug Carrier Systems, 1991, page 92); and non-steroidalanti-inflammatory agents such as diclofenac sodium, indomethacin andphenylbutazone (Yamashita et al., J. Pharm. Pharmacol., 1987, 39, 621).

In some embodiments, oligonucleotide compositions for oral deliverycomprise at least two discrete phases, which phases may compriseparticles, capsules, gel-capsules, microspheres, etc. Each phase maycontain one or more oligonucleotides, penetration enhancers,surfactants, bioadhesives, effervescent agents, or other adjuvant,excipient or diluent. In some embodiments, one phase comprises at leastone oligonucleotide and at least one penetration enhancer. In someembodiments, a first phase comprises at least one oligonucleotide and atleast one penetration enhancer, while a second phase comprises at leastone penetration enhancer. In some embodiments, a first phase comprisesat least one oligonucleotide and at least one penetration enhancer,while a second phase comprises at least one penetration enhancer andsubstantially no oligonucleotide. In some embodiments, at least onephase is compounded with at least one degradation retardant, such as acoating or a matrix, which delays release of the contents of that phase.In some embodiments, a first phase comprises at least oneoligonucleotide and at least one penetration enhancer, while a secondphase comprises at least one penetration enhancer and arelease-retardant. In particular embodiments, an oral oligonucleotidecomposition comprises a first phase comprising particles containing anoligonucleotide and a penetration enhancer, and a second phasecomprising particles coated with a release-retarding agent andcontaining penetration enhancer.

Agents that enhance uptake of oligonucleotides at the cellular level mayalso be added to the pharmaceutical, therapeutic and other compositionsof the present invention. For example, cationic lipids, such asLIPOFECTIN™ reagent (Junichi et al, U.S. Pat. No. 5,705,188), cationicglycerol derivatives, and polycationic molecules, such as polylysine(Lollo et al., International Patent Publication No. WO 97/30731), can beused.

A “pharmaceutical carrier” or “excipient” may be a pharmaceuticallyacceptable solvent, suspending agent or any other pharmacologicallyinert vehicle for delivering one or more nucleic acids to an animal. Theexcipient may be liquid or solid and is selected, with the plannedmanner of administration in mind, so as to provide for the desired bulk,consistency, etc., when combined with a an oligonucleotide and the othercomponents of a given pharmaceutical composition. Typical pharmaceuticalcarriers include, but are not limited to, binding agents (e.g.,pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropylmethylcellulose, etc.); fillers (e.g., lactose and other sugars,microcrystalline cellulose, pectin, gelatin, calcium sulfate, ethylcellulose, polyacrylates or calcium hydrogen phosphate, etc.);lubricants (e.g., magnesium stearate, talc, silica, colloidal silicondioxide, stearic acid, metallic stearates, hydrogenated vegetable oils,corn starch, polyethylene glycols, sodium benzoate, sodium acetate,etc.); disintegrants (e.g., starch, sodium starch glycolate, EXPLOTAB™);and wetting agents (e.g., sodium lauryl sulphate, etc.).

Oral oligonucleotide compositions may additionally contain other adjunctcomponents conventionally found in pharmaceutical compositions, at theirart-established usage levels. Thus, for example, the compositions maycontain additional, compatible, pharmaceutically-active materials suchas, for example, antipruritics, astringents, local anesthetics oranti-inflammatory agents, or may contain additional materials useful inphysically formulating various dosage forms of the composition ofpresent invention, such as dyes, flavoring agents, preservatives,antioxidants, opacifiers, thickening agents and stabilizers. However,such materials, when added, should not unduly interfere with thebiological activities of the components of the compositions of thepresent invention.

Compositions and formulations for parenteral, intrathecal orintraventricular administration may include sterile aqueous solutionswhich may also contain buffers, diluents and other suitable additivessuch as, but not limited to, penetration enhancers, carrier compoundsand other pharmaceutically acceptable carriers or excipients.

The pharmaceutical formulations of the present invention, which mayconveniently be presented in unit dosage form, may be prepared accordingto conventional techniques well known in the pharmaceutical industry.Such techniques include the step of bringing into association the activeingredients with the pharmaceutical carrier(s) or excipient(s). Ingeneral, the formulations are prepared by uniformly and intimatelybringing into association the active ingredients with liquid carriers orfinely divided solid carriers or both, and then, if necessary, shapingthe product.

The compositions of the present invention may be formulated into any ofmany possible dosage forms such as, but not limited to, tablets,capsules, gel capsules, liquid syrups, soft gels, suppositories, andenemas. The compositions of the present invention may also be formulatedas suspensions in aqueous, non-aqueous or mixed media. Aqueoussuspensions may further contain substances which increase the viscosityof the suspension including, for example, sodium carboxymethylcellulose,sorbitol and/or dextran. The suspension may also contain stabilizers.

Pharmaceutical compositions of the present invention include, but arenot limited to, foams, solutions, emulsions, and liposome-containingformulations. These compositions may be generated from a variety ofcomponents that include, but are not limited to, preformed liquids,self-emulsifying solids and self-emulsifying semisolids. Thepharmaceutical compositions and formulations of the present inventionmay comprise one or more penetration enhancers, carriers, excipients orother active or inactive ingredients.

In one embodiment of the present invention the pharmaceuticalcompositions may be formulated and used as foams. Pharmaceutical foamsinclude formulations such as, but not limited to, emulsions,microemulsions, creams, jellies and liposomes. While basically similarin nature these formulations vary in the components and the consistencyof the final product. The preparation of such compositions andformulations is generally known to those skilled in the pharmaceuticaland formulation arts and may be applied to the formulation of thecompositions of the present invention.

The compounds of the present invention may be prepared and formulated asemulsions. Emulsions are typically heterogeneous systems of one liquiddispersed in another in the form of droplets usually exceeding 0.1 μm indiameter (Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger andBanker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p.199; Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger andBanker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., Volume 1, p.245; Block in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker(Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 2, p. 335;Higuchi et al., in Remington's Pharmaceutical Sciences, Mack PublishingCo., Easton, Pa., 1985, p. 301). Emulsions are often biphasic systemscomprising of two immiscible liquid phases intimately mixed anddispersed with each other. In general, emulsions may be eitherwater-in-oil (w/o) or of the oil-in-water (o/w) variety. When an aqueousphase is finely divided into and dispersed as minute droplets into abulk oily phase the resulting composition is called a water-in-oil (w/o)emulsion. Alternatively, when an oily phase is finely divided into anddispersed as minute droplets into a bulk aqueous phase the resultingcomposition is called an oil-in-water (o/w) emulsion. Emulsions maycontain additional components in addition to the dispersed phases andthe active drug which may be present as a solution in either the aqueousphase, oily phase or itself as a separate phase. Pharmaceuticalexcipients such as emulsifiers, stabilizers, dyes, and anti-oxidants mayalso be present in emulsions as needed. Pharmaceutical emulsions mayalso be multiple emulsions that are comprised of more than two phasessuch as, for example, in the case of oil-in-water-in-oil (o/w/o) andwater-in-oil-in-water (w/o/w) emulsions. Such complex formulations oftenprovide certain advantages that simple binary emulsions do not. Multipleemulsions in which individual oil droplets of an o/w emulsion enclosesmall water droplets constitute a w/o/w emulsion. Likewise a system ofoil droplets enclosed in globules of water stabilized in an oilycontinuous provides an o/w/o emulsion.

Often, the dispersed or discontinuous phase of the emulsion is welldispersed into the external or continuous phase and maintained in thisform through the means of emulsifiers or the viscosity of theformulation. Either of the phases of the emulsion may be a semisolid ora solid, as is the case of emulsion-style ointment bases and creams.Other means of stabilizing emulsions entail the use of emulsifiers thatmay be incorporated into either phase of the emulsion. Emulsifiers maybroadly be classified into four categories: synthetic surfactants,naturally occurring emulsifiers, absorption bases, and finely dispersedsolids (Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger andBanker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p.199).

Synthetic surfactants, also known as surface active agents, have foundwide applicability in the formulation of emulsions and have beenreviewed in the literature (Rieger, in Pharmaceutical Dosage Forms,Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., NewYork, N.Y., volume 1, p. 285; Idson, in Pharmaceutical Dosage Forms,Lieberman, Rieger and Banker (Eds.), Marcel Dekker, Inc., New York,N.Y., 1988, volume 1, p. 199). Surfactants are typically amphiphilic andcomprise a hydrophilic and a hydrophobic portion. The ratio of thehydrophilic to the hydrophobic nature of the surfactant has been termedthe hydrophile/lipophile balance (HLB) and is a valuable tool incategorizing and selecting surfactants in the preparation offormulations. Surfactants may be classified into different classes basedon the nature of the hydrophilic group: nonionic, anionic, cationic andamphoteric (Rieger, in Pharmaceutical Dosage Forms, Lieberman, Riegerand Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1,p. 285).

Naturally occurring emulsifiers used in emulsion formulations includelanolin, beeswax, phosphatides, lecithin and acacia. Absorption basespossess hydrophilic properties such that they can soak up water to formw/o emulsions yet retain their semisolid consistencies, such asanhydrous lanolin and hydrophilic petrolatum. Finely divided solids havealso been used as good emulsifiers especially in combination withsurfactants and in viscous preparations. These include polar inorganicsolids, such as heavy metal hydroxides, nonswelling clays such asbentonite, attapulgite, hectorite, kaolin, montmorillonite, colloidalaluminum silicate and colloidal magnesium aluminum silicate, pigmentsand nonpolar solids such as carbon or glyceryl tristearate.

A large variety of non-emulsifying materials are also included inemulsion formulations and contribute to the properties of emulsions.These include fats, oils, waxes, fatty acids, fatty alcohols, fattyesters, humectants, hydrophilic colloids, preservatives and antioxidants(Block, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker(Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 335;Idson, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker(Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199).

Hydrophilic colloids or hydrocolloids include naturally occurring gumsand synthetic polymers such as polysaccharides (for example, acacia,agar, alginic acid, carrageenan, guar gum, karaya gum, and tragacanth),cellulose derivatives (for example, carboxymethylcellulose andcarboxypropylcellulose), and synthetic polymers (for example, carbomers,cellulose ethers, and carboxyvinyl polymers). These disperse or swell inwater to form colloidal solutions that stabilize emulsions by formingstrong interfacial films around the dispersed-phase droplets and byincreasing the viscosity of the external phase.

Since emulsions often contain a number of ingredients such ascarbohydrates, proteins, sterols and phosphatides that may readilysupport the growth of microbes, these formulations often incorporatepreservatives. Commonly used preservatives included in emulsionformulations include methyl paraben, propyl paraben, quaternary ammoniumsalts, benzalkonium chloride, esters of p-hydroxybenzoic acid, and boricacid. Antioxidants are also commonly added to emulsion formulations toprevent deterioration of the formulation. Antioxidants used may be freeradical scavengers such as tocopherols, alkyl gallates, butylatedhydroxyanisole, butylated hydroxytoluene, or reducing agents such asascorbic acid and sodium metabisulfite, and antioxidant synergists suchas citric acid, tartaric acid, and lecithin.

The application of emulsion formulations via dermatological, oral andparenteral routes and methods for their manufacture have been reviewedin the literature (Idson, in Pharmaceutical Dosage Forms, Lieberman,Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., New York, N.Y.,volume 1, p. 199). Emulsion formulations for oral delivery have beenvery widely used because of reasons of ease of formulation, efficacyfrom an absorption and bioavailability standpoint. (Rosoff, inPharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988,Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245; Idson, inPharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988,Marcel Dekker, Inc., New York, N.Y., volume 1, p. 199). Mineral-oil baselaxatives, oil-soluble vitamins and high fat nutritive preparations areamong the materials that have commonly been administered orally as o/wemulsions.

In one embodiment of the present invention, the compositions ofoligonucleotides are formulated as microemulsions. A microemulsion maybe defined as a system of water, oil and amphiphile which is a singleoptically isotropic and thermodynamically stable liquid solution(Rosoff, in Pharmaceutical Dosage Forms, Lieberman, Rieger and Banker(Eds.), 1988, Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245).Typically microemulsions are systems that are prepared by firstdispersing an oil in an aqueous surfactant solution and then adding asufficient amount of a fourth component, generally an intermediatechain-length alcohol to form a transparent system. Therefore,microemulsions have also been described as thermodynamically stable,isotropically clear dispersions of two immiscible liquids that arestabilized by interfacial films of surface-active molecules (Leung andShah, in: Controlled Release of Drugs: Polymers and Aggregate Systems,Rosoff, M., Ed., 1989, VCH Publishers, New York, pages 185-215).Microemulsions commonly are prepared via a combination of three to fivecomponents that include oil, water, surfactant, cosurfactant andelectrolyte. Whether the microemulsion is of the water-in-oil (w/o) oran oil-in-water (o/w) type is dependent on the properties of the oil andsurfactant used and on the structure and geometric packing of the polarheads and hydrocarbon tails of the surfactant molecules (Schott, inRemington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa.,1985, p. 271).

The phenomenological approach utilizing phase diagrams has beenextensively studied and has yielded a comprehensive knowledge, to oneskilled in the art, of how to formulate microemulsions (Rosoff, inPharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988,Marcel Dekker, Inc., New York, N.Y., volume 1, p. 245; Block, inPharmaceutical Dosage Forms, Lieberman, Rieger and Banker (Eds.), 1988,Marcel Dekker, Inc., New York, N.Y., volume 1, p. 335). Compared toconventional emulsions, microemulsions offer the advantage ofsolubilizing water-insoluble drugs in a formulation of thermodynamicallystable droplets that are formed spontaneously.

Surfactants used in the preparation of microemulsions include, but arenot limited to, ionic surfactants, non-ionic surfactants, Brij 96,polyoxyethylene oleyl ethers, polyglycerol fatty acid esters,tetraglycerol monolaurate (ML310), tetraglycerol monooleate (MO310),hexaglycerol monooleate (PO310), hexaglycerol pentaoleate (PO500),decaglycerol monocaprate (MCA750), decaglycerol monooleate (MO750),decaglycerol sequioleate (SO750), decaglycerol decaoleate (DAO750),alone or in combination with cosurfactants. The cosurfactant, usually ashort-chain alcohol such as ethanol, 1-propanol, and 1-butanol, servesto increase the interfacial fluidity by penetrating into the surfactantfilm and consequently creating a disordered film because of the voidspace generated among surfactant molecules. Microemulsions may, however,be prepared without the use of cosurfactants and alcohol-freeself-emulsifying microemulsion systems are known in the art. The aqueousphase may typically be, but is not limited to, water, an aqueoussolution of the drug, glycerol, PEG300, PEG400, polyglycerols, propyleneglycols, and derivatives of ethylene glycol. The oil phase may include,but is not limited to, materials such as Captex 300, Captex 355, CapmulMCM, fatty acid esters, medium chain (C8-C12) mono, di, andtri-glycerides, polyoxyethylated glyceryl fatty acid esters, fattyalcohols, polyglycolized glycerides, saturated polyglycolized C₈-C₁₀glycerides, vegetable oils and silicone oil.

Microemulsions are particularly of interest from the standpoint of drugsolubilization and the enhanced absorption of drugs. Lipid basedmicroemulsions (both o/w and w/o) have been proposed to enhance the oralbioavailability of drugs, including peptides (Constantinides et al.,Pharmaceutical Research, 1994, 11, 1385-1390; Ritschel, Meth. Find. Exp.Clin. Pharmacol., 1993, 13, 205). Microemulsions afford advantages ofimproved drug solubilization, protection of drug from enzymatichydrolysis, possible enhancement of drug absorption due tosurfactant-induced alterations in membrane fluidity and permeability,ease of preparation, ease of oral administration over solid dosageforms, improved clinical potency, and decreased toxicity (Constantinideset al., Pharmaceutical Research, 1994, 11, 1385; Ho et al., J. Pharm.Sci., 1996, 85, 138-143). Often microemulsions may form spontaneouslywhen their components are brought together at ambient temperature. Thismay be particularly advantageous when formulating thermolabile drugs,peptides or oligonucleotides. Microemulsions have also been effective inthe transdermal delivery of active components in both cosmetic andpharmaceutical applications. It is expected that the microemulsioncompositions and formulations of the present invention will facilitatethe increased systemic absorption of oligonucleotides from thegastrointestinal tract, as well as improve the local cellular uptake ofoligonucleotides within the gastrointestinal tract, vagina, buccalcavity and other areas of administration.

Microemulsions of the present invention may also contain additionalcomponents and additives such as sorbitan monostearate (Grill 3),Labrasol, and penetration enhancers to improve the properties of theformulation and to enhance the absorption of the oligonucleotides andnucleic acids of the present invention. Penetration enhancers used inthe microemulsions of the present invention may be classified asbelonging to one of five broad categories described herein.

There are many organized surfactant structures besides microemulsionsthat have been studied and used in the formulation of drugs. Theseinclude monolayers, micelles, bilayers and vesicles. Vesicles, such asliposomes, have attracted great interest because of their specificityand the duration of action they offer from the standpoint of drugdelivery.

Formulations of the present invention include liposomal formulations. Asused in the present invention, the term “liposome” means a vesiclecomposed of amphiphilic lipids arranged in a spherical bilayer orbilayers. Liposomes are unilamellar or multilamellar vesicles which havea membrane formed from a lipophilic material and an aqueous interiorthat contains the composition to be delivered.

In order to cross intact mammalian skin, lipid vesicles must passthrough a series of fine pores, each with a diameter less than 50 nm,under the influence of a suitable transdermal gradient. Therefore, it isdesirable to use a liposome which is highly deformable and able to passthrough such fine pores.

Further advantages of liposomes include: liposomes obtained from naturalphospholipids are biocompatible and biodegradable; liposomes canincorporate a wide range of water and lipid soluble drugs; and liposomescan protect encapsulated drugs in their internal compartments frommetabolism and degradation (Rosoff, in Pharmaceutical Dosage Forms,Lieberman, Rieger and Banker (Eds.), 1988, Marcel Dekker, Inc., NewYork, N.Y., volume 1, p. 245). Important considerations in thepreparation of liposome formulations are the lipid surface charge,vesicle size and the aqueous volume of the liposomes.

Liposomes are useful for the transfer and delivery of active ingredientsto the site of action. Because the liposomal membrane is structurallysimilar to biological membranes, when liposomes are applied to a tissue,the liposomes start to merge with the cellular membranes. As the mergingof the liposome and cell progresses, the liposomal contents are emptiedinto the cell where the active agent may act.

Liposomal formulations have been the focus of extensive investigation asthe mode of delivery for many drugs. There is growing evidence that fortopical administration, liposomes present several advantages over otherformulations. Such advantages include reduced side-effects related tohigh systemic absorption of the administered drug, increasedaccumulation of the administered drug at the desired target, and theability to administer a wide variety of drugs, both hydrophilic andhydrophobic, into the skin.

Several reports have detailed the ability of liposomes to deliver agentsincluding high-molecular weight DNA into the skin. Compounds includinganalgesics, antibodies, hormones and high-molecular weight DNAs havebeen administered to the skin. The majority of applications resulted inthe targeting of the upper epidermis.

Liposomes fall into two broad classes, cationic and non-cationic, bothof which are useful for the delivery of DNA, RNA or any nucleicacid-based construct into cells. Cationic liposomes are positivelycharged liposomes which interact with negatively charged DNA moleculesto form a stable complex. The positively charged DNA/liposome complexbinds to the negatively charged cell surface and is internalized in anendosome. Due to the acidic pH within the endosome, the liposomes areruptured, releasing their contents into the cell cytoplasm (Wang et al.,Biochem. Biophys. Res. Commun., 1987, 147, 980-985).

Liposomes which are pH-sensitive or negatively-charged, also known asnon-cationic liposomes, entrap DNA rather than complex with it. Sinceboth the DNA and the lipid are similarly charged, repulsion rather thancomplex formation occurs. Nevertheless, some DNA is entrapped within theaqueous interior of these liposomes. pH-sensitive liposomes have beenused to deliver DNA encoding the thymidine kinase gene to cellmonolayers in culture. Expression of the exogenous gene was detected inthe target cells (Zhou et al., Journal of Controlled Release, 1992, 19,269-274).

One major type of liposomal composition includes phospholipids otherthan naturally-derived phosphatidylcholine. Neutral liposomecompositions, for example, can be formed from dimyristoylphosphatidylcholine (DMPC) or dipalmitoyl phosphatidylcholine (DPPC).Anionic liposome compositions generally are formed from dimyristoylphosphatidylglycerol, while anionic fusogenic liposomes are formedprimarily from dioleoyl phosphatidylethanolamine (DOPE). Another type ofliposomal composition is formed from phosphatidylcholine (PC) such as,for example, soybean PC, and egg PC. Another type is formed frommixtures of phospholipid and/or phosphatidylcholine and/or cholesterol.

Several studies have assessed the topical delivery of liposomal drugformulations to the skin. Application of liposomes containing interferonto guinea pig skin resulted in a reduction of skin herpes sores whiledelivery of interferon via other means (e.g. as a solution or as anemulsion) were ineffective (Weiner et al., Journal of Drug Targeting,1992, 2, 405-410). Further, an additional study tested the efficacy ofinterferon administered as part of a liposomal formulation to theadministration of interferon using an aqueous system, and concluded thatthe liposomal formulation was superior to aqueous administration (duPlessis et al., Antiviral Research, 1992, 18, 259-265).

Non-ionic liposomal systems have also been examined to determine theirutility in the delivery of drugs to the skin, in particular systemscomprising non-ionic surfactant and cholesterol. Non-ionic liposomalformulations comprising the Novasome™ I (glyceryldilaurate/cholesterol/polyoxyethylene-10-stearyl ether) and Novasome™ II(glyceryl distearate/cholesterol/polyoxyethylene-10-stearyl ether)reagents were used to deliver cyclosporin-A into the dermis of mouseskin. Results indicated that such non-ionic liposomal systems wereeffective in facilitating the deposition of cyclosporin-A into differentlayers of the skin (Hu et al. S.T.P. Pharma. Sci., 1994, 4, 6, 466).

Liposomes also include “sterically stabilized” liposomes, a term which,as used herein, refers to liposomes comprising one or more specializedlipids that, when incorporated into liposomes, result in enhancedcirculation lifetimes relative to liposomes lacking such specializedlipids. Examples of sterically stabilized liposomes are those in whichpart of the vesicle-forming lipid portion of the liposome (A) comprisesone or more glycolipids, such as monosialoganglioside G_(M1), or (B) isderivatized with one or more hydrophilic polymers, such as apolyethylene glycol (PEG) moiety. While not wishing to be bound by anyparticular theory, it is thought in the art that, at least forsterically stabilized liposomes containing gangliosides, sphingomyelin,or PEG-derivatized lipids, the enhanced circulation half-life of thesesterically stabilized liposomes derives from a reduced uptake into cellsof the reticuloendothelial system (RES) (Allen et al., FEBS Letters,1987, 223, 42; Wu et al., Cancer Research, 1993, 53, 3765). Liposomesand their uses are further described in U.S. Pat. No. 6,287,860, whichis incorporated herein in its entirety.

Various liposomes comprising one or more glycolipids are known in theart. Papahadjopoulos et al. (Ann. N.Y. Acad. Sci., 1987, 507, 64)reported the ability of monosialoganglioside G_(M1), galactocerebrosidesulfate and phosphatidylinositol to improve blood half-lives ofliposomes. These findings were expounded upon by Gabizon et al. (Proc.Natl. Acad. Sci. USA., 1988, 85, 6949). U.S. Pat. No. 4,837,028 and WO88/04924, both to Allen et al., disclose liposomes comprising (1)sphingomyelin and (2) the ganglioside G_(M1) or a galactocerebrosidesulfate ester. U.S. Pat. No. 5,543,152 (Webb et al.) discloses liposomescomprising sphingomyelin. Liposomes comprising1,2-sn-dimyristoylphosphatidylcholine are disclosed in WO 97/13499 (Limet al.).

Many liposomes comprising lipids derivatized with one or morehydrophilic polymers, and methods of preparation thereof, are known inthe art. Sunamoto et al. (Bull. Chem. Soc. Jpn., 1980, 53, 2778)described liposomes comprising a nonionic detergent, 2C₁₂l5G, thatcontains a PEG moiety. Illum et al. (FEBS Lett., 1984, 167, 79) notedthat hydrophilic coating of polystyrene particles with polymeric glycolsresults in significantly enhanced blood half-lives. Syntheticphospholipids modified by the attachment of carboxylic groups ofpolyalkylene glycols (e.g., PEG) are described by Sears (U.S. Pat. Nos.4,426,330 and 4,534,899). Klibanov et al. (FEBS Lett., 1990, 268, 235)described experiments demonstrating that liposomes comprisingphosphatidylethanolamine (PE) derivatized with PEG or PEG stearate havesignificant increases in blood circulation half-lives. Blume et al.(Biochimica et Biophysica Acta, 1990, 1029, 91) extended suchobservations to other PEG-derivatized phospholipids, e.g., DSPE-PEG,formed from the combination of distearoylphosphatidylethanolamine (DSPE)and PEG. Liposomes having covalently bound PEG moieties on theirexternal surface are described in European Patent No. EP 0 445 131 B1and WO 90/04384 to Fisher. Liposome compositions containing 1-20 molepercent of PE derivatized with PEG, and methods of use thereof, aredescribed by Woodle et al. (U.S. Pat. Nos. 5,013,556 and 5,356,633) andMartin et al. (U.S. Pat. No. 5,213,804 and European Patent No. EP 0 496813 B1). Liposomes comprising a number of other lipid-polymer conjugatesare disclosed in WO 91/05545 and U.S. Pat. No. 5,225,212 (both to Martinet al.) and in WO 94/20073 (Zalipsky et al.) Liposomes comprisingPEG-modified ceramide lipids are described in WO 96/10391 (Choi et al.).U.S. Pat. Nos. 5,540,935 (Miyazaki et al.) and 5,556,948 (Tagawa et al.)describe PEG-containing liposomes that can be further derivatized withfunctional moieties on their surfaces.

International Patent Publication No. WO 96/40062 to Thierry et al.refers to methods for encapsulating high molecular weight nucleic acidsin liposomes. U.S. Pat. No. 5,264,221 to Tagawa et al. refers toprotein-bonded liposomes and asserts that the contents of such liposomesmay include an antisense RNA. U.S. Pat. No. 5,665,710 to Rahman et al.refers to certain methods of encapsulating oligodeoxynucleotides inliposomes. International Patent Publication No. WO 97/04787 to Love etal. refers to liposomes comprising antisense oligonucleotides targetedto the raf gene.

Transfersomes are yet another type of liposome, and are highlydeformable lipid aggregates which are attractive candidates for drugdelivery vehicles. Transfersomes may be described as lipid dropletswhich are so highly deformable that they are easily able to penetratethrough pores which are smaller than the droplet. Transfersomes areadaptable to the environment in which they are used, e.g. they areself-optimizing (adaptive to the shape of pores in the skin),self-repairing, frequently reach their targets without fragmenting, andoften self-loading. To make transfersomes it is possible to add surfaceedge-activators, usually surfactants, to a standard liposomalcomposition. Transfersomes have been used to deliver serum albumin tothe skin. The transfersome-mediated delivery of serum albumin has beenshown to be as effective as subcutaneous injection of a solutioncontaining serum albumin.

Surfactants find wide application in formulations such as emulsions(including microemulsions) and liposomes. The most common way ofclassifying and ranking the properties of the many different types ofsurfactants, both natural and synthetic, is by the use of thehydrophile/lipophile balance (HLB). The nature of the hydrophilic group(also known as the “head”) provides the most useful means forcategorizing the different surfactants used in formulations (Rieger, inPharmaceutical Dosage Forms, Marcel Dekker, Inc., New York, N.Y., 1988,p. 285).

If the surfactant molecule is not ionized, it is classified as anonionic surfactant. Nonionic surfactants find wide application inpharmaceutical and cosmetic products and are usable over a wide range ofpH values.

In general their HLB values range from 2 to about 18 depending on theirstructure. Nonionic surfactants include nonionic esters such as ethyleneglycol esters, propylene glycol esters, glyceryl esters, polyglycerylesters, sorbitan esters, sucrose esters, and ethoxylated esters.Nonionic alkanolamides and ethers such as fatty alcohol ethoxylates,propoxylated alcohols, and ethoxylated/propoxylated block polymers arealso included in this class. The polyoxyethylene surfactants are themost popular members of the nonionic surfactant class.

If the surfactant molecule carries a negative charge when it isdissolved or dispersed in water, the surfactant is classified asanionic. Anionic surfactants include carboxylates such as soaps, acyllactylates, acyl amides of amino acids, esters of sulfuric acid such asalkyl sulfates and ethoxylated alkyl sulfates, sulfonates such as alkylbenzene sulfonates, acyl isethionates, acyl taurates andsulfosuccinates, and phosphates. The most important members of theanionic surfactant class are the alkyl sulfates and the soaps.

If the surfactant molecule carries a positive charge when it isdissolved or dispersed in water, the surfactant is classified ascationic. Cationic surfactants include quaternary ammonium salts andethoxylated amines. The quaternary ammonium salts are the most usedmembers of this class.

If the surfactant molecule has the ability to carry either a positive ornegative charge, the surfactant is classified as amphoteric. Amphotericsurfactants include acrylic acid derivatives, substituted alkylamides,N-alkylbetaines and phosphatides.

The use of surfactants in drug products, formulations and in emulsionshas been reviewed (Rieger, in Pharmaceutical Dosage Forms, MarcelDekker, Inc., New York, N.Y., 1988, p. 285).

In one embodiment, the present invention employs various penetrationenhancers to effect the efficient delivery of nucleic acids,particularly oligonucleotides, to the skin of animals. Most drugs arepresent in solution in both ionized and nonionized forms. However,usually only lipid soluble or lipophilic drugs readily cross cellmembranes. It has been discovered that even non-lipophilic drugs maycross cell membranes if the membrane to be crossed is treated with apenetration enhancer. In addition to aiding the diffusion ofnon-lipophilic drugs across cell membranes, penetration enhancers alsoenhance the permeability of lipophilic drugs.

Other agents may be utilized to enhance the penetration of theadministered nucleic acids, including glycols such as ethylene glycoland propylene glycol, pyrrols such as 2-pyrrol, azones, and terpenessuch as limonene and menthone.

The pharmaceutical formulations and compositions of the presentinvention may also include surfactants. The use of surfactants in drugproducts, formulations and in emulsions is well known in the art.Surfactants and their uses are further described in U.S. Pat. No.6,287,860, which is incorporated herein in its entirety.

One of skill in the art will recognize that formulations are routinelydesigned according to their intended use, i.e., route of administration.

Preferred formulations for topical administration include those in whichthe oligonucleotides of the invention are in admixture with a topicaldelivery agent such as lipids, liposomes, fatty acids, fatty acidesters, steroids, chelating agents and surfactants. Preferred lipids andliposomes include neutral (e.g. dioleoylphosphatidyl DOPE ethanolamine,dimyristoylphosphatidyl choline DMPC, distearolyphosphatidyl choline)negative (e.g. dimyristoylphosphatidyl glycerol DMPG) and cationic (e.g.dioleoyltetramethylaminopropyl DOTAP and dioleoylphosphatidylethanolamine DOTMA).

For topical or other administration, oligonucleotides of the inventionmay be encapsulated within liposomes or may form complexes thereto, inparticular to cationic liposomes. Alternatively, oligonucleotides may becomplexed to lipids, in particular to cationic lipids. Preferred fattyacids and esters, pharmaceutically acceptable salts thereof, and theiruses are further described in U.S. Pat. No. 6,287,860, which isincorporated herein in its entirety Topical formulations are describedin detail in U.S. Pat. No. 6,747,014, which is incorporated herein byreference in its entirety.

Compositions and formulations for oral administration include powders orgranules, microparticulates, nanoparticulates, suspensions or solutionsin water or non-aqueous media, capsules, gel capsules, sachets, tabletsor minitablets. Thickeners, flavoring agents, diluents, emulsifiers,dispersing aids or binders may be desirable. Preferred oral formulationsare those in which oligonucleotides of the invention are administered inconjunction with one or more penetration enhancers surfactants andchelators. Preferred surfactants include fatty acids and/or esters orsalts thereof, bile acids and/or salts thereof. Preferred bileacids/salts and fatty acids and their uses are further described in U.S.Pat. No. 6,287,860, which is incorporated herein in its entirety. Alsopreferred are combinations of penetration enhancers, for example, fattyacids/salts in combination with bile acids/salts. A particularlypreferred combination is the sodium salt of lauric acid, capric acid andUDCA. Further penetration enhancers include polyoxyethylene-9-laurylether, polyoxyethylene-20-cetyl ether. Oligonucleotides of the inventionmay be delivered orally, in granular form including sprayed driedparticles, or complexed to form micro or nanoparticles. Oligonucleotidecomplexing agents and their uses are further described in U.S. Pat. No.6,287,860, which is incorporated herein in its entirety. Oralformulations for oligonucleotides and their preparation are described indetail in U.S. Pat. No. 6,747,014; U.S. Patent Publication No.2003/0027780 (Feb. 6, 2003) and its parent applications; and U.S. patentapplication Ser. No. 09/082,624 (filed May 21, 1998), each of which isincorporated herein by reference in its entirety.

Compositions and formulations for parenteral, intrathecal orintraventricular administration may include sterile aqueous solutionswhich may also contain buffers, diluents and other suitable additivessuch as, but not limited to, penetration enhancers, carrier compoundsand other pharmaceutically acceptable carriers or excipients.

Oligonucleotides may be formulated for delivery in vivo in an acceptabledosage form, e.g. as parenteral or non-parenteral formulations.Parenteral formulations include intravenous (IV), subcutaneous (SC),intraperitoneal (IP), intravitreal and intramuscular (IM) formulations,as well as formulations for delivery via pulmonary inhalation,intranasal administration, topical administration, etc. Non-parenteralformulations include formulations for delivery via the alimentary canal,e.g. oral administration, rectal administration, intrajejunalinstillation, etc. Rectal administration includes administration as anenema or a suppository. Oral administration includes administration as acapsule, a gel capsule, a pill, an elixir, etc.

The compounds of the present invention may also be administered bypulsatile delivery. “Pulsatile delivery” refers to a pharmaceuticalformulation that delivers a first pulse of drug (e.g. an antisensecompound) combined with a penetration enhancer and a second pulse ofpenetration enhancer to promote absorption of drug which is not absorbedupon release with the first pulse of penetration enhancer.

One embodiment of the present invention is a delayed release oralformulation for enhanced intestinal drug absorption, comprising:

(a) a first population of carrier particles comprising said drug and apenetration enhancer, wherein said drug and said penetration enhancerare released at a first location in the intestine; and(b) a second population of carrier particles comprising a penetrationenhancer and a delayed release coating or matrix, wherein thepenetration enhancer is released at a second location in the intestinedownstream from the first location, whereby absorption of the drug isenhanced when the drug reaches the second location.

Alternatively, the penetration enhancer in (a) and (b) is different.This enhancement is obtained by encapsulating at least two populationsof carrier particles. The first population of carrier particlescomprises a biologically active substance and a penetration enhancer,and the second (and optionally additional) population of carrierparticles comprises a penetration enhancer and a delayed release coatingor matrix.

A “first pass effect” that applies to orally administered drugs isdegradation due to the action of gastric acid and various digestiveenzymes. One means of ameliorating first pass clearance effects is toincrease the dose of administered drug, thereby compensating forproportion of drug lost to first pass clearance. This may be readilyachieved with i.v. administration by, for example, simply providing moreof the drug to an animal. However, other factors influence thebioavailability of drugs administered via non-parenteral means. Forexample, a drug may be enzymatically or chemically degraded in thealimentary canal or blood stream and/or may be impermeable orsemipermeable to various mucosal membranes.

These pharmaceutical compositions are capable of enhancing absorption ofbiologically active substances when administered via the rectal,vaginal, nasal or pulmonary routes. Release of the biologically activesubstance can be achieved in any part of the gastrointestinal tract.

Liquid pharmaceutical compositions of oligonucleotide can be prepared bycombining the oligonucleotide with a suitable vehicle, for examplesterile pyrogen free water, or saline solution. Other therapeuticcompounds may optionally be included.

The present invention also contemplates the use of solid particulatecompositions. Such compositions preferably comprise particles ofoligonucleotide that are of respirable size. Such particles can beprepared by, for example, grinding dry oligonucleotide by conventionalmeans, fore example with a mortar and pestle, and then passing theresulting powder composition through a 400 mesh screen to segregatelarge particles and agglomerates. A solid particulate compositioncomprised of an active oligonucleotide can optionally contain adispersant which serves to facilitate the formation of an aerosol, forexample lactose.

In accordance with the present invention, oligonucleotide compositionscan be aerosolized. Aerosolization of liquid particles can be producedby any suitable means, such as with a nebulizer. See, for example, U.S.Pat. No. 4,501,729. Nebulizers are commercially available devices whichtransform solutions or suspensions into a therapeutic aerosol misteither by means of acceleration of a compressed gas, typically air oroxygen, through a narrow venturi orifice or by means of ultrasonicagitation. Suitable nebulizers include those sold by Blairex® under thename PARI LC PLUS, PARI DURA-NEB 2000, PARI -BABY Size, PARI PRONEBCompressor with LC PLUS, PARI WALKHALER Compressor/Nebulizer System,PARI LC PLUS Reusable Nebulizer, and PARI LC Jet+®Nebulizer.

Formulations for use in nebulizers may consist of an oligonucleotide ina liquid, such as sterile, pyragen free water, or saline solution,wherein the oligonucleotide comprises up to about 40% w/w of theformulation. Preferably, the oligonucleotide comprises less than 20%w/w. If desired, further additives such as preservatives (for example,methyl hydroxybenzoate) antioxidants, and flavoring agents can be addedto the composition.

Solid particles comprising an oligonucleotide can also be aerosolizedusing any solid particulate medicament aerosol generator known in theart. Such aerosol generators produce respirable particles, as describedabove, and further produce reproducible metered dose per unit volume ofaerosol. Suitable solid particulate aerosol generators includeinsufflators and metered dose inhalers. Metered dose inhalers are usedin the art and are useful in the present invention. Preferably, liquidor solid aerosols are produced at a rate of from about 10 to 150 litersper minute, more preferably from about 30 to 150 liters per minute, andmost preferably about 60 liters per minute.

Enhanced bioavailability of biologically active substances is alsoachieved via the oral administration of the compositions and methods ofthe present invention.

The compositions of the present invention may additionally contain otheradjunct components conventionally found in pharmaceutical compositions,at their art-established usage levels. Thus, for example, thecompositions may contain additional, compatible, pharmaceutically-activematerials such as, for example, antipruritics, astringents, localanesthetics or anti-inflammatory agents, or may contain additionalmaterials useful in physically formulating various dosage forms of thecompositions of the present invention, such as dyes, flavoring agents,preservatives, antioxidants, opacifiers, thickening agents andstabilizers. However, such materials, when added, should not undulyinterfere with the biological activities of the components of thecompositions of the present invention. The formulations can besterilized and, if desired, mixed with auxiliary agents, e.g.,lubricants, preservatives, stabilizers, wetting agents, emulsifiers,salts for influencing osmotic pressure, buffers, colorings, flavoringsand/or aromatic substances and the like which do not deleteriouslyinteract with the nucleic acid(s) of the formulation.

Aqueous suspensions may contain substances which increase the viscosityof the suspension including, for example, sodium carboxymethylcellulose,sorbitol and/or dextran. The suspension may also contain stabilizers.

Certain embodiments of the invention provide pharmaceutical compositionscontaining one or more oligomeric compounds and one or more otherchemotherapeutic agents which function by a non-antisense mechanism.Examples of such chemotherapeutic agents include but are not limited tocancer chemotherapeutic drugs such as daunorubicin, daunomycin,dactinomycin, doxorubicin, epirubicin, idarubicin, esorubicin,bleomycin, mafosfamide, ifosfamide, cytosine arabinoside,bis-chloroethylnitrosurea, busulfan, mitomycin C, actinomycin D,mithramycin, prednisone, hydroxyprogesterone, testosterone, tamoxifen,dacarbazine, procarbazine, hexamethylmelamine, pentamethylmelamine,mitoxantrone, amsacrine, chlorambucil, methylcyclohexylnitrosurea,nitrogen mustards, melphalan, cyclophosphamide, 6-mercaptopurine,6-thioguanine, cytarabine, 5-azacytidine, hydroxyurea, deoxycoformycin,4-hydroxyperoxycyclophosphoramide, 5-fluorouracil (5-FU),5-fluorodeoxyuridine (5-FUdR), methotrexate (MTX), colchicine, taxol,vincristine, vinblastine, etoposide (VP-16), trimetrexate, irinotecan,topotecan, gemcitabine, teniposide, cisplatin and diethylstilbestrol(DES). When used with the compounds of the invention, suchchemotherapeutic agents may be used individually (e.g., 5-FU andoligonucleotide), sequentially (e.g., 5-FU and oligonucleotide for aperiod of time followed by MTX and oligonucleotide), or in combinationwith one or more other such chemotherapeutic agents (e.g., 5-FU, MTX andoligonucleotide, or 5-FU, radiotherapy and oligonucleotide).Anti-inflammatory drugs, including but not limited to nonsteroidalanti-inflammatory drugs and corticosteroids, and antiviral drugs,including but not limited to ribivirin, vidarabine, acyclovir andganciclovir, may also be combined in compositions of the invention.Combinations of antisense compounds and other non-antisense drugs arealso within the scope of this invention. Two or more combined compoundsmay be used together or sequentially.

In another related embodiment, compositions of the invention may containone or more antisense compounds, particularly oligonucleotides, targetedto a first nucleic acid and one or more additional antisense compoundstargeted to a second nucleic acid target. Alternatively, compositions ofthe invention may contain two or more antisense compounds targeted todifferent regions of the same nucleic acid target. Numerous examples ofantisense compounds are known in the art. Two or more combined compoundsmay be used together or sequentially.

H. Dosing

The formulation of therapeutic compositions and their subsequentadministration (dosing) is believed to be within the skill of those inthe art. Dosing is dependent on severity and responsiveness of thedisease state to be treated, with the course of treatment lasting fromseveral days to several months, or until a cure is effected or adiminution of the disease state is achieved. Optimal dosing schedulescan be calculated from measurements of drug accumulation in the body ofthe patient. Persons of ordinary skill can easily determine optimumdosages, dosing methodologies and repetition rates. Optimum dosages mayvary depending on the relative potency of individual oligonucleotides,and can generally be estimated based on EC₅₀s found to be effective inin vitro and in vivo animal models. In general, dosage is from 0.01 μgto 100 g per kg of body weight, from 0.1 μg to 10 g per kg of bodyweight, from 1.0 μg to 1 g per kg of body weight, from 10.0 μg to 100 mgper kg of body weight, from 100 μg to 10 mg per kg of body weight, orfrom 1 mg to 5 mg per kg of body weight, and may be given once or moredaily, weekly, monthly or yearly, or even once every 2 to 20 years.Persons of ordinary skill in the art can easily estimate repetitionrates for dosing based on measured residence times and concentrations ofthe drug in bodily fluids or tissues. Following successful treatment, itmay be desirable to have the patient undergo maintenance therapy toprevent the recurrence of the disease state, wherein the oligonucleotideis administered in maintenance doses, ranging from 0.01 ug to 100 g perkg of body weight, once or more daily, to once every 20 years.

The effects of treatments with therapeutic compositions can be assessedfollowing collection of tissues or fluids from a patient or subjectreceiving said treatments. It is known in the art that a biopsy samplecan be procured from certain tissues without resulting in detrimentaleffects to a patient or subject. In certain embodiments, a tissue andits constituent cells comprise, but are not limited to, blood (e.g.,hematopoietic cells, such as human hematopoietic progenitor cells, humanhematopoietic stem cells, CD34⁺ cells CD4⁺ cells), lymphocytes and otherblood lineage cells, bone marrow, breast, cervix, colon, esophagus,lymph node, muscle, peripheral blood, oral mucosa and skin. In otherembodiments, a fluid and its constituent cells comprise, but are notlimited to, blood, urine, semen, synovial fluid, lymphatic fluid andcerebro-spinal fluid. Tissues or fluids procured from patients can beevaluated for expression levels of the target mRNA or protein.Additionally, the mRNA or protein expression levels of other genes knownor suspected to be associated with the specific disease state, conditionor phenotype can be assessed. mRNA levels can be measured or evaluatedby real-time PCR, Northern blot, in situ hybridization or DNA arrayanalysis. Protein levels can be measured or evaluated by ELISA,immunoblotting, quantitative protein assays, protein activity assays(for example, caspase activity assays) immunohistochemistry orimmunocytochemistry. Furthermore, the effects of treatment can beassessed by measuring biomarkers associated with the disease orcondition in the aforementioned tissues and fluids, collected from apatient or subject receiving treatment, by routine clinical methodsknown in the art. These biomarkers include but are not limited to:glucose, cholesterol, lipoproteins, triglycerides, free fatty acids andother markers of glucose and lipid metabolism; lipoprotein(a) or Lp(a)or apolipoprotein B; liver transaminases, bilirubin, albumin, blood ureanitrogen, creatine and other markers of kidney and liver function;interleukins, tumor necrosis factors, intracellular adhesion molecules,C-reactive protein and other markers of inflammation; testosterone,estrogen and other hormones; tumor markers; vitamins, minerals andelectrolytes.

While the present invention has been described with specificity inaccordance with certain of its preferred embodiments, the followingexamples serve only to illustrate the invention and are not intended tolimit the same. Each of the references, GENBANK® accession numbers, andthe like recited in the present application is incorporated herein byreference in its entirety.

EXAMPLES Example 1 Synthesis of Nucleoside Phosphoramidites

The following compounds, including amidites and their intermediates wereprepared as described in U.S. Pat. No. 6,426,220 and InternationalPatent Publication No. WO 02/36743; 5′-O-Dimethoxytrityl-thymidineintermediate for 5-methyl dC amidite,5′-O-Dimethoxytrityl-2′-deoxy-5-methylcytidine intermediate for5-methyl-dC amidite,5′-O-Dimethoxytrityl-2′-deoxy-N4-benzoyl-5-methylcytidine penultimateintermediate for 5-methyl dC amidite,[5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-deoxy-N⁴-benzoyl-5-methylcytidin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite(5-methyl dC amidite), 2′-Fluorodeoxyadenosine, 2′-Fluorodeoxyguanosine,2′-Fluorouridine, 2′-Fluorodeoxycytidine, 2′-O-(2-Methoxyethyl) modifiedamidites, 2′-O-(2-methoxyethyl)-5-methyluridine intermediate,5′-O-DMT-2′-O-(2-methoxyethyl)-5-methyluridine penultimate intermediate,[5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl)-5-methyluridin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite(MOE T amidite),5′-O-Dimethoxytrityl-2′-O-(2-methoxyethyl)-5-methylcytidineintermediate,5′-O-dimethoxytrityl-2′-O-(2-methoxyethyl)-N⁴-benzoyl-5-methyl-cytidinepenultimate intermediate,[5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl)-N⁴-benzoyl-5-methylcytidin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite(MOE 5-Me-C amidite),[5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl)-N⁶-benzoyladenosin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite(MOE A amidite),[5′-O-(4,4′-Dimethoxytriphenylmethyl)-2′-O-(2-methoxyethyl)-N⁴-isobutyrylguanosin-3′-O-yl]-2-cyanoethyl-N,N-diisopropylphosphoramidite(MOE G amidite), 2′-O-(Aminooxyethyl) nucleoside amidites and2′-O-(dimethylaminooxyethyl) nucleoside amidites,2′-(Dimethylaminooxyethoxy) nucleoside amidites,5′-O-tert-Butyldiphenylsilyl-O²-2′-anhydro-5-methyluridine,5′-O-tert-Butyldiphenylsilyl-2′-O-(2-hydroxyethyl)-5-methyluridine,2′-O-([2-phthalimidoxy)ethyl]-5′-t-butyldiphenylsilyl-5-methyluridine,5′-O-tert-butyldiphenylsilyl-2′-O-([2-formadoximinooxy)ethyl]-5-methyluridine,5′-O-tert-Butyldiphenylsilyl-2′-O—[N,Ndimethylaminooxyethyl]-5-methyluridine,2′-O-(dimethylaminooxyethyl)-5-methyluridine,5′-O-DMT-2′-O-(dimethylaminooxyethyl)-5-methyluridine,5′-O-DMT-2′-O-(2-N,N-dimethylaminooxyethyl)-5-methyluridine-3′-[(2-cyanoethyl)-N,N-diisopropylphosphoramidite],2′-(Aminooxyethoxy) nucleoside amidites,N2-isobutyryl-6-O-diphenylcarbamoyl-2′-O-(2-ethylacetyl)-5′-O-(4,4′-dimethoxytrityl)guanosine-3′-[(2-cyanoethyl)-N,N-diisopropylphosphoramidite],2′-dimethylaminoethoxyethoxy (2′-DMAEOE) nucleoside amidites,2′-O-[2(2-N,N-dimethylaminoethoxy)ethyl]-5-methyl uridine,5′-O-dimethoxytrityl-2′-O-[2(2-N,N-dimethylaminoethoxy)-ethyl)]-5-methyluridine and5′-O-Dimethoxytrityl-2′-O-[2(2-N,N-dimethylaminoethoxy)-ethyl)]-5-methyluridine-3′-O-(cyanoethyl-N,N-diisopropyl)phosphoramidite.

Example 2 Oligonucleotide and Oligonucleoside Synthesis

The antisense compounds used in accordance with this invention may beconveniently and routinely made through the well-known technique ofsolid phase synthesis. Equipment for such synthesis is sold by severalvendors including, for example, Applied Biosystems (Foster City,Calif.). Any other means for such synthesis known in the art mayadditionally or alternatively be employed. It is well known to usesimilar techniques to prepare oligonucleotides such as thephosphorothioates and alkylated derivatives.

Oligonucleotides: Unsubstituted and substituted phosphodiester (P═O)oligonucleotides are synthesized on an automated DNA synthesizer(Applied Biosystems model 394) using standard phosphoramidite chemistrywith oxidation by iodine.

Phosphorothioates (P═S) are synthesized similar to phosphodiesteroligonucleotides with the following exceptions: thiation was effected byutilizing a 10% w/v solution of 3,H-1,2-benzodithiole-3-one 1,1-dioxidein acetonitrile for the oxidation of the phosphite linkages. Thethiation reaction step time was increased to 180 sec and preceded by thenormal capping step. After cleavage from the CPG column and deblockingin concentrated ammonium hydroxide at 55° C. (12-16 hr), theoligonucleotides were recovered by precipitating with >3 volumes ofethanol from a 1 M NH₄OAc solution. Phosphinate oligonucleotides areprepared as described in U.S. Pat. No. 5,508,270, herein incorporated byreference.

Alkyl phosphonate oligonucleotides are prepared as described in U.S.Pat. No. 4,469,863, herein incorporated by reference.

3′-Deoxy-3′-methylene phosphonate oligonucleotides are prepared asdescribed in U.S. Pat. No. 5,610,289 or 5,625,050, herein incorporatedby reference.

Phosphoramidite oligonucleotides are prepared as described in U.S. Pat.No. 5,256,775 or 5,366,878, herein incorporated by reference.

Alkylphosphonothioate oligonucleotides are prepared as described inInternational Patent Application Nos. PCT/US94/00902 and PCT/US93/06976(published as International Patent Publication Nos. WO 94/17093 and WO94/02499, respectively), herein incorporated by reference.

3′-Deoxy-3′-amino phosphoramidate oligonucleotides are prepared asdescribed in U.S. Pat. No. 5,476,925, herein incorporated by reference.

Phosphotriester oligonucleotides are prepared as described in U.S. Pat.No. 5,023,243, herein incorporated by reference.

Borano phosphate oligonucleotides are prepared as described in U.S. Pat.Nos. 5,130,302 and 5,177,198, both herein incorporated by reference.

Oligonucleosides: Methylenemethylimino linked oligonucleosides, alsoidentified as MMI linked oligonucleosides, methylenedimethylhydrazolinked oligonucleosides, also identified as MDH linked oligonucleosides,and methylenecarbonylamino linked oligonucleosides, also identified asamide-3 linked oligonucleosides, and methyleneaminocarbonyl linkedoligonucleosides, also identified as amide-4 linked oligonucleosides, aswell as mixed backbone compounds having, for instance, alternating MMIand P═O or P═S linkages are prepared as described in U.S. Pat. Nos.5,378,825, 5,386,023, 5,489,677, 5,602,240 and 5,610,289, all of whichare herein incorporated by reference.

Formacetal and thioformacetal linked oligonucleosides are prepared asdescribed in U.S. Pat. Nos. 5,264,562 and 5,264,564, herein incorporatedby reference.

Ethylene oxide linked oligonucleosides are prepared as described in U.S.Pat. No. 5,223,618, herein incorporated by reference.

Example 3 RNA Synthesis

In general, RNA synthesis chemistry is based on the selectiveincorporation of various protecting groups at strategic intermediaryreactions. Although one of ordinary skill in the art will understand theuse of protecting groups in organic synthesis, a useful class ofprotecting groups includes silyl ethers. In particular bulky silylethers are used to protect the 5′-hydroxyl in combination with anacid-labile orthoester protecting group on the 2′-hydroxyl. This set ofprotecting groups is then used with standard solid-phase synthesistechnology. It is important to lastly remove the acid labile orthoesterprotecting group after all other synthetic steps. Moreover, the earlyuse of the silyl protecting groups during synthesis ensures facileremoval when desired, without undesired deprotection of 2′ hydroxyl.

Following this procedure for the sequential protection of the5′-hydroxyl in combination with protection of the 2′-hydroxyl byprotecting groups that are differentially removed and are differentiallychemically labile, RNA oligonucleotides were synthesized.

RNA oligonucleotides are synthesized in a stepwise fashion. Eachnucleotide is added sequentially (3′- to 5′-direction) to a solidsupport-bound oligonucleotide. The first nucleoside at the 3′-end of thechain is covalently attached to a solid support. The nucleotideprecursor, a ribonucleoside phosphoramidite, and activator are added,coupling the second base onto the 5″-end of the first nucleoside. Thesupport is washed and any unreacted 5″-hydroxyl groups are capped withacetic anhydride to yield 5′-acetyl moieties. The linkage is thenoxidized to the more stable and ultimately desired P(V) linkage. At theend of the nucleotide addition cycle, the 5″-silyl group is cleaved withfluoride. The cycle is repeated for each subsequent nucleotide.

Following synthesis, the methyl protecting groups on the phosphates arecleaved in 30 minutes utilizing 1 Mdisodium-2-carbamoyl-2-cyanoethylene-1,1-dithiolate trihydrate (S₂Na₂)in DMF. The deprotection solution is washed from the solid support-boundoligonucleotide using water. The support is then treated with 40%methylamine in water for 10 minutes at 55° C. This releases the RNAoligonucleotides into solution, deprotects the exocyclic amines, andmodifies the 2′-groups. The oligonucleotides can be analyzed by anionexchange HPLC at this stage.

The 2″-orthoester groups are the last protecting groups to be removed.The ethylene glycol monoacetate orthoester protecting group developed byDharmacon Research, Inc. (Lafayette, Colo.), is one example of a usefulorthoester protecting group which, has the following importantproperties. It is stable to the conditions of nucleoside phosphoramiditesynthesis and oligonucleotide synthesis. However, after oligonucleotidesynthesis the oligonucleotide is treated with methylamine which not onlycleaves the oligonucleotide from the solid support but also removes theacetyl groups from the orthoesters. The resulting 2-ethyl-hydroxylsubstituents on the orthoester are less electron withdrawing than theacetylated precursor. As a result, the modified orthoester becomes morelabile to acid-catalyzed hydrolysis. Specifically, the rate of cleavageis approximately 10 times faster after the acetyl groups are removed.Therefore, this orthoester possesses sufficient stability in order to becompatible with oligonucleotide synthesis and yet, when subsequentlymodified, permits deprotection to be carried out under relatively mildaqueous conditions compatible with the final RNA oligonucleotideproduct.

Additionally, methods of RNA synthesis are well known in the art(Scaringe, S. A. Ph.D. Thesis, University of Colorado, 1996; Scaringe,S. A., et al., J. Am. Chem. Soc., 1998, 120, 11820-11821; Matteucci, M.D. and Caruthers, M. H. J. Am. Chem. Soc., 1981, 103, 3185-3191;Beaucage, S. L. and Caruthers, M. H. Tetrahedron Lett., 1981, 22,1859-1862; Dahl, B. J., et al., Acta Chem. Scand, 1990, 44, 639-641;Reddy, M. P., et al., Tetrahedrom Lett., 1994, 25, 4311-4314; Wincott,F. et al., Nucleic Acids Res., 1995, 23, 2677-2684; Griffin, B. E., etal., Tetrahedron, 1967, 23, 2301-2313; Griffin, B. E., et al.,Tetrahedron, 1967, 23, 2315-2331).

RNA antisense compounds (RNA oligonucleotides) of the present inventioncan be synthesized by the methods herein or purchased from DharmaconResearch, Inc (Lafayette, Colo.). Once synthesized, complementary RNAantisense compounds can then be annealed by methods known in the art toform double stranded (duplexed) antisense compounds. For example,duplexes can be formed by combining 30 μl of each of the complementarystrands of RNA oligonucleotides (50 μM RNA oligonucleotide solution) and15 μl of 5× annealing buffer (100 mM potassium acetate, 30 mM HEPES-KOHpH 7.4, 2 mM magnesium acetate) followed by heating for 1 minute at 90°C., then 1 hour at 37° C. The resulting duplexed antisense compounds canbe used in kits, assays, screens, or other methods to investigate therole of a target nucleic acid, or for diagnostic or therapeuticpurposes.

Example 4 Synthesis of Chimeric Compounds

Chimeric oligonucleotides, oligonucleosides or mixedoligonucleotides/oligonucleosides of the invention can be of severaldifferent types. These include a first type wherein the “gap” segment oflinked nucleosides is positioned between 5′ and 3′ “wing” segments oflinked nucleosides and a second “open end” type wherein the “gap”segment is located at either the 3′ or the 5′ terminus of the oligomericcompound. Oligonucleotides of the first type are also known in the artas “gapmers” or gapped oligonucleotides. Oligonucleotides of the secondtype are also known in the art as “hemimers” or “wingmers”.

[2′-O-M]-[2′-deoxy]-[2′-O-Me] Chimeric Phosphorothioate Oligonucleotides

Chimeric oligonucleotides having 2′-O-alkyl phosphorothioate and2′-deoxy phosphorothioate oligo-nucleotide segments are synthesizedusing an Applied Biosystems automated DNA synthesizer Model 394, asabove. Oligonucleotides are synthesized using the automated synthesizerand 2′-deoxy-5′-dimethoxytrityl-3′-O-phosphoramidite for the DNA portionand 5′-dimethoxytrityl-2′-O-methyl-3′-O-phosphoramidite for 5′ and 3′wings. The standard synthesis cycle is modified by incorporatingcoupling steps with increased reaction times for the5′-dimethoxytrityl-2′-O-methyl-3′-O-phosphoramidite. The fully protectedoligonucleotide is cleaved from the support and deprotected inconcentrated ammonia (NH₄OH) for 12-16 hr at 55° C. The deprotectedoligo is then recovered by an appropriate method (precipitation, columnchromatography, volume reduced in vacuo and analyzedspectrophotometrically for yield and for purity by capillaryelectrophoresis and by mass spectrometry).

[2′-O-(2-Methoxyethyl)]-[2′-deoxy]-[2′-O-(Methoxyethyl)] ChimericPhosphorothioate Oligonucleotides

[2′-O-(2-methoxyethyl)]-[2′-deoxy]-[-2′-O-(methoxyethyl)] chimericphosphorothioate oligonucleotides were prepared as per the procedureabove for the 2′-O-methyl chimeric oligonucleotide, with thesubstitution of 2′-O-(methoxyethyl) amidites for the 2′-O-methylamidites.

[2′-O-(2-Methoxyethyl)Phosphodiester]-[2′-deoxyPhosphorothioate]-[2′-O-(2-Methoxyethyl) Phosphodiester] ChimericOligonucleotides

[2′-O-(2-methoxyethyl phosphodiester]-[2′-deoxyphosphorothioate]-[2′-O-(methoxyethyl) phosphodiester] chimericoligonucleotides are prepared as per the above procedure for the2′-O-methyl chimeric oligonucleotide with the substitution of2′-O-(methoxyethyl) amidites for the 2′-O-methyl amidites, oxidationwith iodine to generate the phosphodiester internucleotide linkageswithin the wing portions of the chimeric structures and sulfurizationutilizing 3,H-1,2 benzodithiole-3-one 1,1 dioxide (Beaucage Reagent) togenerate the phosphorothioate internucleotide linkages for the centergap.

Other chimeric oligonucleotides, chimeric oligonucleosides and mixedchimeric oligonucleotides/oligonucleosides are synthesized according toU.S. Pat. No. 5,623,065, herein incorporated by reference.

Example 5 Design and Screening of Duplexed Antisense Compounds TargetingDiacylglycerol Acyltransferase 2

In accordance with the present invention, a series of nucleic acidduplexes, also known as double-strand RNAs (dsRNAs) or small interferingRNAs (siRNAs), comprising the antisense compounds of the presentinvention and their complements can be designed to target diacylglycerolacyltransferase 2. The nucleobase sequence of the antisense strand ofthe duplex comprises at least an 8-nucleobase portion of anoligonucleotide in Table 1. The ends of the strands may be modified bythe addition of one or more natural or modified nucleobases to form anoverhang. The sense strand of the dsRNA is then designed and synthesizedas the complement of the antisense strand and may also containmodifications or additions to either terminus. For example, in oneembodiment, both strands of the dsRNA duplex would be complementary overthe central nucleobases, each having overhangs at one or both termini.The antisense and sense strands of the duplex comprise from about 17 to25 nucleotides, or from about 19 to 23 nucleotides. Alternatively, theantisense and sense strands comprise 20, 21 or 22 nucleotides.

For example, a duplex comprising an antisense strand having the sequenceCGAGAGGCGGACGGGACCG (SEQ ID NO: 489) and having a two-nucleobaseoverhang of deoxythymidine(dT) has the following structure (AntisenseSEQ ID NO: 490 and Complement SEQ ID NO: 491):

Overhangs can range from 1 to 6 nucleobases and these nucleobases may ormay not be complementary to the target nucleic acid. One of skill in theart will understand that the overhang may be 1, 2, 3, 4, 5 or 6nucleobases in length. In another embodiment, the duplexes may have anoverhang on only one terminus.

In another embodiment, a duplex comprising an antisense strand havingthe same sequence CGAGAGGCGGACGGGACCG (SEQ ID NO: 489) may be preparedwith blunt ends (no single stranded overhang) as shown (Antisense SEQ IDNO: 489 and Complement SEQ ID NO: 492):

The RNA duplex can be unimolecular or bimolecular; i.e., the two strandscan be part of a single molecule or may be separate molecules.

RNA strands of the duplex can be synthesized by methods disclosed hereinor purchased from Dharmacon Research Inc., (Lafayette, Colo.). Oncesynthesized, the complementary strands are annealed. The single strandsare aliquoted and diluted to a concentration of 50 μM. Once diluted, 30μL of each strand is combined with 15 μL of a 5× solution of annealingbuffer. The final concentration of said buffer is 100 mM potassiumacetate, 30 mM HEPES-KOH pH 7.4, and 2 mM magnesium acetate. The finalvolume is 75 μL. This solution is incubated for 1 minute at 90° C. andthen centrifuged for 15 seconds. The tube is allowed to sit for 1 hourat 37° C. at which time the dsRNA duplexes are used in experimentation.The final concentration of the dsRNA duplex is 20 μM. This solution canbe stored frozen (−20° C.) and freeze-thawed up to 5 times.

Once prepared, the duplexed antisense compounds are evaluated for theirability to modulate diacylglycerol acyltransferase 2 expression.

When cells reached 80% confluency, they are treated with duplexedantisense compounds of the invention. For cells grown in 96-well plates,wells are washed once with 200 μL OPTI-MEM-1 reduced-serum medium (GibcoBRL) and then treated with 130 μL of OPTI-MEM-1 containing 12 μg/mLLIPOFECTINT™ reagent (Gibco BRL) and the desired duplex antisensecompound at a final concentration of 200 nM. After 5 hours of treatment,the medium is replaced with fresh medium. Cells are harvested 16 hoursafter treatment, at which time RNA is isolated and target reductionmeasured by RT-PCR.

Example 6 Oligonucleotide Isolation

After cleavage from the controlled pore glass solid support anddeblocking in concentrated ammonium hydroxide at 55° C. for 12-16 hours,the oligonucleotides or oligonucleosides are recovered by precipitationout of 1 M NH₄OAc with >3 volumes of ethanol. Synthesizedoligonucleotides were analyzed by electrospray mass spectroscopy(molecular weight determination) and by capillary gel electrophoresisand judged to be at least 70% full-length material. The relative amountsof phosphorothioate and phosphodiester linkages obtained in thesynthesis was determined by the ratio of correct molecular weightrelative to the −16 amu product (+/−32+/−48). For some studiesoligonucleotides were purified by HPLC, as described by Chiang et al.,J. Biol. Chem. 1991, 266, 18162-18171. Results obtained withHPLC-purified material were similar to those obtained with non-HPLCpurified material.

Example 7 Oligonucleotide Synthesis 96 Well Plate Format

Oligonucleotides were synthesized via solid phase P(III) phosphoramiditechemistry on an automated synthesizer capable of assembling 96 sequencessimultaneously in a 96-well format. Phosphodiester internucleotidelinkages were afforded by oxidation with aqueous iodine.Phosphorothioate internucleotide linkages were generated bysulfurization utilizing 3,H-1,2 benzodithiole-3-one 1,1 dioxide(Beaucage Reagent) in anhydrous acetonitrile. Standard base-protectedbeta-cyanoethyl-diiso-propyl phosphoramidites were purchased fromcommercial vendors (e.g. PE-Applied Biosystems, Foster City, Calif., orPharmacia, Piscataway, N.J.). Non-standard nucleosides are synthesizedas per standard or patented methods. They are utilized as base protectedbeta-cyanoethyldiisopropyl phosphoramidites.

Oligonucleotides were cleaved from support and deprotected withconcentrated NH₄OH at elevated temperature (55-60° C.) for 12-16 hoursand the released product then dried in vacuo. The dried product was thenre-suspended in sterile water to afford a master plate from which allanalytical and test plate samples are then diluted utilizing roboticpipettors.

Example 8 Oligonucleotide Analysis 96-Well Plate Format

The concentration of oligonucleotide in each well was assessed bydilution of samples and UV absorption spectroscopy. The full-lengthintegrity of the individual products was evaluated by capillaryelectrophoresis (CE) in either the 96-well format (Beckman P/ACE™ MDQapparatus) or, for individually prepared samples, on a commercial CEapparatus (e.g., Beckman P/ACE™ 5000, ABI 270 apparatus). Base andbackbone composition was confirmed by mass analysis of the compoundsutilizing electrospray-mass spectroscopy. All assay test plates werediluted from the master plate using single and multi-channel roboticpipettors. Plates were judged to be acceptable if at least 85% of thecompounds on the plate were at least 85% full length.

Example 9 Cell Culture and Oligonucleotide Treatment

The effect of antisense compounds on target nucleic acid expression canbe tested in any of a variety of cell types provided that the targetnucleic acid is present at measurable levels. This can be routinelydetermined using, for example, PCR or Northern blot analysis. Thefollowing cell types are provided for illustrative purposes, but othercell types can be routinely used, provided that the target is expressedin the cell type chosen. This can be readily determined by methodsroutine in the art, for example Northern blot analysis, ribonucleaseprotection assays, or real-time PCR.

T-24 Cells:

The human transitional cell bladder carcinoma cell line T-24 wasobtained from the American Type Culture Collection (ATCC) (Manassas,Va.). T-24 cells were routinely cultured in complete McCoy's 5A basalmedia (Invitrogen Corporation, Carlsbad, Calif.) supplemented with 10%fetal bovine serum (Invitrogen Corporation, Carlsbad, Calif.),penicillin 100 units per mL, and streptomycin 100 micrograms per mL(Invitrogen Corporation, Carlsbad, Calif.). Cells were routinelypassaged by trypsinization and dilution when they reached 90%confluence. Cells were seeded into 96-well plates (Falcon-Primaria#353872) at a density of 7000 cells/well for use in RT-PCR analysis.

For Northern blotting or other analysis, cells may be seeded onto 100 mmor other standard tissue culture plates and treated similarly, usingappropriate volumes of medium and oligonucleotide.

A549 Cells:

The human lung carcinoma cell line A549 was obtained from the AmericanType Culture Collection (ATCC) (Manassas, Va.). A549 cells wereroutinely cultured in DMEM basal media (Invitrogen Corporation,Carlsbad, Calif.) supplemented with 10% fetal bovine serum (InvitrogenCorporation, Carlsbad, Calif.), penicillin 100 units per mL, andstreptomycin 100 micrograms per mL (Invitrogen Corporation, Carlsbad,Calif.). Cells were routinely passaged by trypsinization and dilutionwhen they reached 90% confluence.

NHDF Cells:

Human neonatal dermal fibroblast (NHDF) were obtained from the CloneticsCorporation (Walkersville, Md.). NHDFs were routinely maintained inFibroblast Growth Medium (Clonetics Corporation, Walkersville, Md.)supplemented as recommended by the supplier. Cells were maintained forup to 10 passages as recommended by the supplier.

HEK Cells:

Human embryonic keratinocytes (HEK) were obtained from the CloneticsCorporation (Walkersville, Md.). HEKs were routinely maintained inKeratinocyte Growth Medium (Clonetics Corporation, Walkersville, Md.)formulated as recommended by the supplier. Cells were routinelymaintained for up to 10 passages as recommended by the supplier.

3T3-L1 Cells:

The mouse embryonic adipocyte-like cell line 3T3-L1 was obtained fromthe American Type Culture Collection (Manassas, Va.). 3T3-L1 cells wereroutinely cultured in DMEM, high glucose (Invitrogen Corporation,Carlsbad, Calif.) supplemented with 10% fetal bovine serum (InvitrogenCorporation, Carlsbad, Calif.). Cells were routinely passaged bytrypsinization and dilution when they reached 80% confluence. Cells wereseeded into 96-well plates (Falcon-Primaria #3872) at a density of 4000cells/well for use in RT-PCR analysis.

For Northern blotting or other analyses, cells may be seeded onto 100 mmor other standard tissue culture plates and treated similarly, usingappropriate volumes of medium and oligonucleotide.

Primary Mouse Hepatocytes:

Primary mouse hepatocytes were prepared from CD-1 mice purchased fromCharles River Labs. Primary mouse hepatocytes were routinely cultured inHepatocyte Attachment Media supplemented with 10% fetal bovine serum, 1%penicillin/streptomycin, 1% antibiotic-antimitotic (Invitrogen LifeTechnologies, Carlsbad, Calif.) and 10 nM bovine insulin (Sigma-Aldrich,St. Louis, Mo.). Cells were seeded into 96-well plates (Falcon-Primaria#3872) coated with 0.1 mg/ml collagen at a density of approximately10,000 cells/well for use in oligomeric compound transfectionexperiments.

Treatment with Antisense Compounds:

When cells reached 65-75% confluency, they were treated witholigonucleotide. For cells grown in 96-well plates, wells were washedonce with 100 μL OPTI-MEM™-1 reduced-serum medium (InvitrogenCorporation, Carlsbad, Calif.) and then treated with 130 μL of theOPTI-MEM™-1 medium containing 2.5 or 3 μg/mL LIPOFECTINT™ reagent(Invitrogen Corporation, Carlsbad, Calif.) per 100 nM ofoligonucleotide. Cells are treated and data are obtained in triplicate.After 4-7 hours of treatment at 37° C., the medium was replaced withfresh medium. Cells were harvested 16-24 hours after oligonucleotidetreatment.

The concentration of oligonucleotide used varies from cell line to cellline. To determine the optimal oligonucleotide concentration for aparticular cell line, the cells are treated with a positive controloligonucleotide at a range of concentrations. For human cells thepositive control oligonucleotide is selected from either ISIS 13920(TCCGTCATCGCTCCTCAGGG, SEQ ID NO: 1) which is targeted to human H-ras,or ISIS 18078, (GTGCGCGCGAGCCCGAAATC, SEQ ID NO: 2) which is targeted tohuman Jun-N-terminal kinase-2 (JNK2). Both controls are2′-O-methoxyethyl gapmers (2′-O-methoxyethyls shown in bold) with aphosphorothioate backbone. For mouse or rat cells the positive controloligonucleotide is ISIS 15770, ATGCATTCTGCCCCCAAGGA, SEQ ID NO: 3, a2′-O-methoxyethyl gapmer (2′-O-methoxyethyls shown in bold) with aphosphorothioate backbone which is targeted to both mouse and rat c-raf.The concentration of positive control oligonucleotide that results in80% inhibition of c-H-ras (for ISIS 13920), JNK2 (for ISIS 18078) orc-raf (for ISIS 15770) mRNA is then utilized as the screeningconcentration for new oligonucleotides in subsequent experiments forthat cell line. If 80% inhibition is not achieved, the lowestconcentration of positive control oligonucleotide that results in 60%inhibition of c-H-ras, JNK2 or c-raf mRNA is then utilized as theoligonucleotide screening concentration in subsequent experiments forthat cell line. If 60% inhibition is not achieved, that particular cellline is deemed as unsuitable for oligonucleotide transfectionexperiments. The concentrations of antisense oligonucleotides usedherein are from 50 nM to 300 nM.

Example 10 Analysis of Oligonucleotide Inhibition of DiacylglycerolAcyltransferase 2 Expression

Antisense modulation of diacylglycerol acyltransferase 2 expression canbe assayed in a variety of ways known in the art. For example,diacylglycerol acyltransferase 2 mRNA levels can be quantitated by,e.g., Northern blot analysis, competitive polymerase chain reaction(PCR), or real-time PCR. Quantitative real-time PCR is presentlypreferred. RNA analysis can be performed on total cellular RNA orpoly(A)+ mRNA. The preferred method of RNA analysis of the presentinvention is the use of total cellular RNA as described in otherexamples herein. Methods of RNA isolation are well known in the art.Northern blot analysis is also routine in the art. Real-timequantitative (PCR) can be conveniently accomplished using thecommercially available ABI PRISM™ 7600, 7700, or 7900 Sequence DetectionSystem, available from PE-Applied Biosystems, Foster City, Calif. andused according to manufacturer's instructions.

Protein levels of diacylglycerol acyltransferase 2 can be quantitated ina variety of ways well known in the art, such as immunoprecipitation,Western blot analysis (immunoblotting), enzyme-linked immunosorbentassay (ELISA) or fluorescence-activated cell sorting (FACS). Antibodiesdirected to diacylglycerol acyltransferase 2 can be identified andobtained from a variety of sources, such as the MSRS catalog ofantibodies (Aerie Corporation, Birmingham, Mich.), or can be preparedvia conventional monoclonal or polyclonal antibody generation methodswell known in the art.

Example 11 Design of Phenotypic Assays for the Use of DiacylglycerolAcyltransferase 2 Inhibitors

Once diacylglycerol acyltransferase 2 inhibitors have been identified bythe methods disclosed herein, the compounds are further investigated inone or more phenotypic assays, each having measurable endpointspredictive of efficacy in the treatment of a particular disease state orcondition. Phenotypic assays, kits and reagents for their use are wellknown to those skilled in the art and are herein used to investigate therole and/or association of diacylglycerol acyltransferase 2 in healthand disease. Representative phenotypic assays, which can be purchasedfrom any one of several commercial vendors, include those fordetermining cell viability, cytotoxicity, proliferation or cell survival(Molecular Probes, Eugene, Oreg.; PerkinElmer, Boston, Mass.),protein-based assays including enzymatic assays (Panvera, LLC, Madison,Wis.; BD Biosciences, Franklin Lakes, N.J.; Oncogene Research Products,San Diego, Calif.), cell regulation, signal transduction, inflammation,oxidative processes and apoptosis (Assay Designs Inc., Ann Arbor,Mich.), triglyceride accumulation (Sigma-Aldrich, St. Louis, Mo.),angiogenesis assays, tube formation assays, cytokine and hormone assaysand metabolic assays (Chemicon International Inc., Temecula, Calif.;Amersham Biosciences, Piscataway, N.J.).

In one non-limiting example, cells determined to be appropriate for aparticular phenotypic assay (i.e., MCF-7 cells selected for breastcancer studies; adipocytes for obesity studies) are treated withdiacylglycerol acyltransferase 2 inhibitors identified from the in vitrostudies as well as control compounds at optimal concentrations which aredetermined by the methods described above. At the end of the treatmentperiod, treated and untreated cells are analyzed by one or more methodsspecific for the assay to determine phenotypic outcomes and endpoints.

Phenotypic endpoints include changes in cell morphology over time ortreatment dose as well as changes in levels of cellular components suchas proteins, lipids, nucleic acids, hormones, saccharides or metals.Measurements of cellular status which include pH, stage of the cellcycle, intake or excretion of biological indicators by the cell, arealso endpoints of interest.

Analysis of the expression of one or more genes in the cell aftertreatment is also used as an indicator of the efficacy or potency of thediacylglycerol acyltransferase 2 inhibitors. Hallmark genes, or thosegenes suspected to be associated with a specific disease state,condition, or phenotype, are measured in both treated and untreatedcells.

Example 12 RNA Isolation

Poly(A)+ mRNA Isolation

Poly(A)+ mRNA was isolated according to Miura et al., (Clin. Chem.,1996, 42, 1758-1764). Other methods for poly(A)+ mRNA isolation areroutine in the art. Briefly, for cells grown on 96-well plates, growthmedium was removed from the cells and each well was washed with 200 μLcold PBS. 60 μL lysis buffer (10 mM Tris-HCl, pH 7.6, 1 mM EDTA, 0.5 MNaCl, 0.5% NP-40, 20 mM vanadyl-ribonucleoside complex) was added toeach well, the plate was gently agitated and then incubated at roomtemperature for five minutes. 55 μL of lysate was transferred to Oligod(T) coated 96-well plates (AGCT Inc., Irvine Calif.). Plates wereincubated for 60 minutes at room temperature, washed 3 times with 200 μLof wash buffer (10 mM Tris-HCl pH 7.6, 1 mM EDTA, 0.3 M NaCl). After thefinal wash, the plate was blotted on paper towels to remove excess washbuffer and then air-dried for 5 minutes. 60 μL of elution buffer (5 mMTris-HCl pH 7.6), preheated to 70° C., was added to each well, the platewas incubated on a 90° C. hot plate for 5 minutes, and the eluate wasthen transferred to a fresh 96-well plate.

Cells grown on 100 mm or other standard plates may be treated similarly,using appropriate volumes of all solutions.

Total RNA Isolation

Total RNA was isolated using an RNEASY™ 96 kit and buffers purchasedfrom Qiagen, Inc. (Valencia, Calif.) following the manufacturer'srecommended procedures. Briefly, for cells grown on 96-well plates,growth medium was removed from the cells and each well was washed with200 μL cold PBS. 150 μL Buffer RLT was added to each well and the platevigorously agitated for 20 seconds. 150 μL of 70% ethanol was then addedto each well and the contents mixed by pipetting three times up anddown. The samples were then transferred to the RNEASY™ 96 well plateattached to a QIAVAC™ manifold fitted with a waste collection tray andattached to a vacuum source. Vacuum was applied for 1 minute. 500 μL ofBuffer RW1 was added to each well of the RNEASY™ 96 plate and incubatedfor 15 minutes and the vacuum was again applied for 1 minute. Anadditional 500 μL of Buffer RW1 was added to each well of the RNEASY™ 96plate and the vacuum was applied for 2 minutes. 1 mL of Buffer RPE wasthen added to each well of the RNEASY™ 96 plate and the vacuum appliedfor a period of 90 seconds. The Buffer RPE wash was then repeated andthe vacuum was applied for an additional 3 minutes. The plate was thenremoved from the QIAVAC™ manifold and blotted dry on paper towels. Theplate was then re-attached to the QIAVAC™ manifold fitted with acollection tube rack containing 1.2 mL collection tubes. RNA was theneluted by pipetting 140 μL of RNase free water into each well,incubating 1 minute, and then applying the vacuum for 3 minutes.

The repetitive pipetting and elution steps may be automated using aQIAGEN® Bio-Robot™ 9604 instrument (Qiagen, Inc., Valencia Calif.).Essentially, after lysing of the cells on the culture plate, the plateis transferred to the robot deck where the pipetting, DNase treatmentand elution steps are carried out.

Example 13 Real-Time Quantitative PCR Analysis of DiacylglycerolAcyltransferase 2 mRNA Levels

Quantitation of diacylglycerol acyltransferase 2 mRNA levels wasaccomplished by real-time quantitative PCR using the ABI PRISM™ 7600,7700, or 7900 Sequence Detection System (PE-Applied Biosystems, FosterCity, Calif.) according to manufacturer's instructions. This is aclosed-tube, non-gel-based, fluorescence detection system which allowshigh-throughput quantitation of polymerase chain reaction (PCR) productsin real-time. As opposed to standard PCR in which amplification productsare quantitated after the PCR is completed, products in real-timequantitative PCR are quantitated as they accumulate. This isaccomplished by including in the PCR reaction an oligonucleotide probethat anneals specifically between the forward and reverse PCR primers,and contains two fluorescent dyes. A reporter dye (e.g., FAM or JOE,obtained from either PE-Applied Biosystems, Foster City, Calif., OperonTechnologies Inc., Alameda, Calif. or Integrated DNA Technologies Inc.,Coralville, Iowa) is attached to the 5′ end of the probe and a quencherdye (e.g., TAMRA, obtained from either PE-Applied Biosystems, FosterCity, Calif., Operon Technologies Inc., Alameda, Calif. or IntegratedDNA Technologies Inc., Coralville, Iowa) is attached to the 3′ end ofthe probe. When the probe and dyes are intact, reporter dye emission isquenched by the proximity of the 3′ quencher dye. During amplification,annealing of the probe to the target sequence creates a substrate thatcan be cleaved by the 5′-exonuclease activity of Taq polymerase. Duringthe extension phase of the PCR amplification cycle, cleavage of theprobe by Taq polymerase releases the reporter dye from the remainder ofthe probe (and hence from the quencher moiety) and a sequence-specificfluorescent signal is generated. With each cycle, additional reporterdye molecules are cleaved from their respective probes, and thefluorescence intensity is monitored at regular intervals by laser opticsbuilt into the ABI PRISM™ Sequence Detection System. In each assay, aseries of parallel reactions containing serial dilutions of mRNA fromuntreated control samples generates a standard curve that is used toquantitate the percent inhibition after antisense oligonucleotidetreatment of test samples.

Prior to quantitative PCR analysis, primer-probe sets specific to thetarget gene being measured are evaluated for their ability to be“multiplexed” with a GAPDH amplification reaction. In multiplexing, boththe target gene and the internal standard gene GAPDH are amplifiedconcurrently in a single sample. In this analysis, mRNA isolated fromuntreated cells is serially diluted. Each dilution is amplified in thepresence of primer-probe sets specific for GAPDH only, target gene only(“single-plexing”), or both (multiplexing). Following PCR amplification,standard curves of GAPDH and target mRNA signal as a function ofdilution are generated from both the single-plexed and multiplexedsamples. If both the slope and correlation coefficient of the GAPDH andtarget signals generated from the multiplexed samples fall within 10% oftheir corresponding values generated from the single-plexed samples, theprimer-probe set specific for that target is deemed multiplexable. Othermethods of PCR are also known in the art.

Gene target quantities are obtained by real-time PCR. Prior to thereal-time PCR, isolated RNA is subjected to a reverse transcriptase (RT)reaction, for the purpose of generating complementary DNA (cDNA). Thereal-time PCR is then performed on the resulting cDNA. Reversetranscriptase and PCR reagents were obtained from InvitrogenCorporation, (Carlsbad, Calif.). RT, real-time PCR reactions werecarried out by adding 20 μL PCR cocktail (2.5×PCR buffer minus MgCl₂,6.6 mM MgCl₂, 375 μM each of dATP, dCTP, dCTP and dGTP, 375 nM each offorward primer and reverse primer, 125 nM of probe, 4 Units RNaseinhibitor, 1.25 Units PLATINUM® Taq polymerase, 5 Units MuLV reversetranscriptase, and 2.5×ROX dye) to 96-well plates containing 30 μL totalRNA solution (20-200 ng). The RT reaction was carried out by incubationfor 30 minutes at 48° C. Following a 10 minute incubation at 95° C. toactivate the PLATINUM® Taq polymerase, 40 cycles of a two-step PCRprotocol were carried out: 95° C. for 15 seconds (denaturation) followedby 60° C. for 1.5 minutes (annealing/extension). The method of obtaininggene target quantities by RT, real-time PCR is often referred to assimply real-time PCR.

Gene target quantities obtained by real-time PCR are normalized usingeither the expression level of GAPDH, a gene whose expression isconstant, or by quantifying total RNA using the RIBOGREEN™ reagent(Molecular Probes, Inc. Eugene, Oreg.). GAPDH expression is quantifiedby real time real-time PCR, by being run simultaneously with the target,multiplexing, or separately. Total RNA is quantified using RIBOGREEN™RNA quantification reagent (Molecular Probes, Inc. Eugene, Oreg.).Methods of RNA quantification by the RIBOGREEN™ reagent are taught inJones, L. J., et al, (Analytical Biochemistry, 1998, 265, 368-374).

In this assay, 170 μL of RiboGreen™ working reagent (the RIBOGREEN™reagent diluted 1:350 in 10 mM Tris-HCl, 1 mM EDTA, pH 7.5) was pipettedinto a 96-well plate containing 30 μL purified, cellular RNA. The platewas read in a CytoFluor 4000 apparatus (PE Applied Biosystems) withexcitation at 485 nm and emission at 530 nm.

Probes and primers to human diacylglycerol acyltransferase 2 weredesigned to hybridize to a human diacylglycerol acyltransferase 2sequence, using published sequence information (GENBANK® accessionnumber NM_(—)032564.2, incorporated herein as SEQ ID NO: 4). For humandiacylglycerol acyltransferase 2 the PCR primers were:

forward primer: CATACGGCCTTACCTGGCTACA (SEQ ID NO: 5)reverse primer: CAGACATCAGGTACTCCCTCAACA (SEQ ID NO: 6) and the PCRprobe was: FAM-TGGCAGGCAACTTCCGAATGCC-TAMRA(SEQ ID NO: 7) where FAM is the fluorescent dye and TAMRA is thequencher dye. For human GAPDH the PCR primers were:forward primer: GAAGGTGAAGGTCGGAGTC(SEQ ID NO:8)reverse primer: GAAGATGGTGATGGGATTTC (SEQ ID NO:9) and the PCR probewas: 5′ JOE-CAAGCTTCCCGTTCTCAGCC-TAMRA 3′ (SEQ ID NO: 10) where JOE isthe fluorescent reporter dye and TAMRA is the quencher dye.

Probes and primers to mouse diacylglycerol acyltransferase 2 weredesigned to hybridize to a mouse diacylglycerol acyltransferase 2sequence, using published sequence information (GENBANK® accessionnumber AK002443.1, incorporated herein as SEQ ID NO:11). For mousediacylglycerol acyltransferase 2 the PCR primers were:

forward primer: ACTCTGGAGGTTGGCACCAT (SEQ ID NO:12)reverse primer: GGGTGTGGCTCAGGAGGAT (SEQ ID NO: 13) and the PCR probewas: FAM-CAGCGTTGCTCTGGCGCA-TAMRA(SEQ ID NO: 14) where FAM is the fluorescent reporter dye and TAMRA isthe quencher dye. For mouse GAPDH the PCR primers were:forward primer: GGCAAATTCAACGGCACAGT(SEQ ID NO:15)reverse primer: GGGTCTCGCTCCTGGAAGAT(SEQ ID NO:16) and the PCR probewas: 5′ JOE-AAGGCCGAGAATGGGAAGCTTGTCATC-TAMRA 3′ (SEQ ID NO: 17) whereJOE is the fluorescent reporter dye and TAMRA is the quencher dye.

Example 14 Northern Blot Analysis of Diacylglycerol Acyltransferase 2mRNA Levels

Eighteen hours after antisense treatment, cell monolayers were washedtwice with cold PBS and lysed in 1 mL RNAZOL™ reagent (TEL-TEST “B”Inc., Friendswood, Tex.). Total RNA was prepared followingmanufacturer's recommended protocols. Twenty micrograms of total RNA wasfractionated by electrophoresis through 1.2% agarose gels containing1.1% formaldehyde using a MOPS buffer system (AMRESCO, Inc. Solon,Ohio). RNA was transferred from the gel to HYBONDT™-N+ nylon membranes(Amersham Pharmacia Biotech, Piscataway, N.J.) by overnight capillarytransfer using a Northern/Southern Transfer buffer system (TEL-TEST “B”Inc., Friendswood, Tex.). RNA transfer was confirmed by UVvisualization. Membranes were fixed by UV cross-linking using aSTRATALINKER™ UV Crosslinker 2400 instrument (Stratagene, Inc, La Jolla,Calif.) and then probed using QUICKHYB™ hybridization solution(Stratagene, La Jolla, Calif.) using manufacturer's recommendations forstringent conditions.

To detect human diacylglycerol acyltransferase 2, a human diacylglycerolacyltransferase 2 specific probe was prepared by PCR using the forwardprimer CATACGGCCTTACCTGGCTACA (SEQ ID NO: 5) and the reverse primerCAGACATCAGGTACTCCCTCAACA (SEQ ID NO: 6). To normalize for variations inloading and transfer efficiency membranes were stripped and probed forhuman glyceraldehyde-3-phosphate dehydrogenase (GAPDH) RNA (Clontech,Palo Alto, Calif.).

To detect mouse diacylglycerol acyltransferase 2, a mouse diacylglycerolacyltransferase 2 specific probe was prepared by PCR using the forwardprimer ACTCTGGAGGTTGGCACCAT (SEQ ID NO: 12) and the reverse primerGGGTGTGGCTCAGGAGGAT (SEQ ID NO: 13). To normalize for variations inloading and transfer efficiency membranes were stripped and probed formouse glyceraldehyde-3-phosphate dehydrogenase (GAPDH) RNA (Clontech,Palo Alto, Calif.).

Hybridized membranes were visualized and quantitated usingPHOSPHORIMAGER™ and IMAGEQUANT™ Software V3.3 (Molecular Dynamics,Sunnyvale, Calif.). Data was normalized to GAPDH levels in untreatedcontrols.

Example 15 Antisense Inhibition of Human Diacylglycerol Acyltransferase2 Expression by Chimeric Phosphorothioate Oligonucleotides Having 2′-MOEWings and a Deoxy Gap

In accordance with the present invention, a series of antisensecompounds was designed to target different regions of the humandiacylglycerol acyltransferase 2 RNA, using published sequences(GENBANK® accession number NM_(—)032564.2, incorporated herein as SEQ IDNO: 4, nucleotides 5669186 to 5712008 of the nucleotide sequence withthe GenBank accession number NT_(—)033927.5, incorporated herein as SEQID NO: 18). The compounds are shown in Table 1. “Target site” indicatesthe first (5′-most) nucleotide number on the particular target sequenceto which the compound binds. All compounds in Table 1 are chimericoligonucleotides (“gapmers”) 20 nucleotides in length, composed of acentral “gap” region consisting of ten 2′-deoxynucleotides, which isflanked on both sides (5′ and 3′ directions) by five-nucleotide “wings”.The wings are composed of 2′-O-methoxyethyl (2′-MOE) nucleotides. Theinternucleoside (backbone) linkages are phosphorothioate (P═S)throughout the oligonucleotide. All cytidine residues are5-methylcytidines. The compounds were analyzed for their effect on humandiacylglycerol acyltransferase 2 mRNA levels by quantitative real-timePCR as described in other examples herein. Data are averages from threeexperiments in which A549 cells were treated with 125 nM of theantisense oligonucleotides of the present invention. If present, “N.D.”indicates “no data”. ISIS 18078 (SEQ ID NO: 2) was used in this assay asa negative control.

TABLE 1 Inhibition of human diacylglycerol acyltransferase2 mRNA levels by chimeric phosphorothioateoligonucleotides having 2′-MOE wings and a deoxy gap TARGET SEQ ISISSEQ ID TARGET % ID # REGION NO SITE SEQUENCE (5′ to 3′) INHIB NO 217310Coding  4 579 ctcctgccacctttcttggg 79 20 217312 Coding  4 639tggatgggaaagtagtctcg 82 21 217313 Coding  4 644 ccagctggatgggaaagtag 3422 217314 Coding  4 649 cttcaccagctggatgggaa 40 23 217315 Coding  4 654tgtgtcttcaccagctggat 86 24 217316 Coding  4 659 ggttgtgtgtcttcaccagc 8825 217317 Coding  4 664 cagcaggttgtgtgtcttca 93 26 217318 Coding  4 669gtggtcagcaggttgtgtgt 74 27 217319 Coding  4 674 tcctggtggtcagcaggttg 8428 217320 Coding  4 679 atagttcctggtggtcagca 90 29 217321 Coding  4 684aagatatagttcctggtggt 77 30 217322 Coding  4 689 atccaaagatatagttcctg 7331 217323 Coding  4 694 gtggtatccaaagatatagt 70 32 217324 Coding  4 723aaggcacccaggcccatgat 74 33 217325 Coding  4 846 cctccagacatcaggtactc 7334 217328 Coding  4 909 gcattgccactcccattctt 89 35 217329 Coding  4 914tgatagcattgccactccca 88 36 217330 Coding  4 919 gatgatgatagcattgccac 7737 217331 Coding  4 924 accacgatgatgatagcatt 77 38 217333 Coding  4 963ttgccaggcatggagctcag 79 39 217336 Coding  4 1110 tggacccatcggccccagga 7240 217337 Coding  4 1115 tcttctggacccatcggccc 76 41 217338 Coding  41120 gaacttcttctggacccatc 43 42 217339 Coding  4 1125ttctggaacttcttctggac 62 43 217341 Coding  4 1197 ggcaccagcccccaggtgtc 6844 217342 Coding  4 1202 agtagggcaccagcccccag 54 45 217343 Coding  41207 cttggagtagggcaccagcc 69 46 217346 Coding  4 1309cagggcctccatgtacatgg 81 47 217347 Coding  4 1314 ttcaccagggcctccatgta 5448 217348 Coding  4 1319 agagcttcaccagggcctcc 83 49 217353 3′UTR  4 1469aacccacagacacccatgac 65 50 217354 3′UTR  4 1474 taaataacccacagacaccc 4051 217355 3′UTR  4 1479 tcttttaaataacccacaga 47 52 334165 intron 1821985 acaaaagagcatcctcctca 64 53 334166 intron 18 23110actataaatgcttcagtcca 78 54 334167 exon: intron 18 31175ttgcacttacctttcttggg 8 55 334168 exon:intron 18 31611agcactttacctggatggga 63 56 334169 intron 18 33686 tcagtgaaatgaggcagatg84 57 334170 intron 18 35303 ctcaaaagaggtgacatcaa 72 58 334171exon:intron 18 37412 ggattcttacctccagacat 22 59 334172 intron:exon 1839106 caggtcagctctggaaggga 47 60 334173 intron 18 37108ttcccctggacctccatggg 76 61 334174 5′UTR  4 46 gtggcgcgagagaaacagcc 82 62334175 5′UTR  4 134 gccagggcttcgcgcagagc 75 63 334176 Start Codon  4 222agggtcttcatggctgaagc 53 64 334177 Coding  4 246 aggaccccggagtaggcggc 4565 334178 Coding  4 441 acccactggagcactgagat 83 66 334179 Coding  4 855gggcagatacctccagacat 28 67 334180 Coding  4 987 cggttccgcagggtgactgc 7268 334181 Stop Codon 4  1387 aaggctggctcagttcacct 78 69 334182 3′UTR  41401 gggagttggccccgaaggct 64 70 334183 3′UTR  4 1414gctggttcctccagggagtt 81 71 334184 3′UTR  4 1449 acttccaaatttacagagca 7272 334185 3′UTR  4 1584 ccacctagaacagggcaagc 80 73 334186 3′UTR  4 1635gggaagaagagaggttagct 35 74 334187 3′UTR  4 1647 tcacttcaggaagggaagaa 6375 334188 3′UTR  4 1679 ccttcttccccaagaagact 51 76 334184 3′UTR  4 1707ctaactggtccaagtcacta 82 77 334190 3′UTR  4 1724 ggcaaaaagtgaatcatcta 7678 334191 3′UTR  4 1743 ttcgcctctcatccctaggg 13 79 334142 3′UTR  4 1763ggcttgtatgagaagtggct 77 80 334193 3′UTR  4 1802 tttcaggactagacgagcgt 8281 334144 3′UTR  4 1946 ctccgatatgagtgactagg 85 82 334145 3′UTR  4 1969ctcatcctggaggccagtcc 72 83 334196 3′UTR  4 1974 ccatcctcatcctggaggcc 5084 334197 3′UTR  4 1989 gtgtcattgccacccccatc 49 85 334198 3′UTR  4 2055acctagctcatggtggcggc 67 86 334199 3′UTR  4 2067 accagttactccacctagct 7387 334200 3′UTR  4 2088 gtcatcagccacccaagaaa 73 88 334201 3′UTR  4 2125gtgctccaggccaaggctga 75 89 334202 3′UTR  4 2137 accagtaagcatgtgctcca 8490 334203 3′UTR  4 2143 gaggccaccagtaagcatgt 65 91 334204 3′UTR  4 2150gtaaactgaggccaccagta 82 92 334205 3′UTR  4 2184 cttcctcacatccagaatct 2293 334206 3′UTR  4 2220 tgctcagaaggccaggcccc 89 94 334207 3′UTR  4 2242acctcctttggaactaatct 76 95 334208 3′UTR  4 2269 gaaaagtgaggcttgggttc 4496 334209 3′UTR  4 2367 aaaagtctgacatggtgcaa 75 97

As shown in Table 1, SEQ ID Nos: 20, 21, 23, 24, 25, 26, 27, 28, 29, 30,31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48,49, 50, 51, 52, 53, 54, 56, 57, 58, 60, 61, 62, 63, 64, 65, 66, 68, 69,70, 71, 72, 73, 75, 76, 77, 78, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89,90, 91, 92, 94, 95, 96 and 97 demonstrated at least 40% inhibition ofhuman diacylglycerol acyltransferase 2 expression in this assay and aretherefore preferred. More preferred are SEQ ID Nos: 65, 26, 29 and 35.The target regions to which these preferred sequences are complementaryare herein referred to as “preferred target segments” and are thereforepreferred for targeting by compounds of the present invention. Thesepreferred target segments are shown in Table 3. These sequences areshown to contain thymine (T) but one of skill in the art will appreciatethat thymine (T) is generally replaced by uracil (U) in RNA sequences.The sequences represent the reverse complement of the preferredantisense compounds shown in Table 1. “Target site” indicates the first(5′-most) nucleotide number on the particular target nucleic acid towhich the oligonucleotide binds. Also shown in Table 3 is the species inwhich each of the preferred target segments was found.

Example 16 Antisense Inhibition of Mouse Diacylglycerol Acyltransferase2 Expression by Chimeric Phosphorothioate Oligonucleotides Having 2′-MOEWings and a Deoxy Gap

In accordance with the present invention, a series of antisensecompounds was designed to target different regions of the mousediacylglycerol acyltransferase 2 RNA, using published sequences(GENBANK® accession number AK002443.1, incorporated herein as SEQ ID NO:11). The compounds are shown in Table 2. “Target site” indicates thefirst (5′-most) nucleotide number on the particular target nucleic acidto which the compound binds. All compounds in Table 2 are chimericoligonucleotides (“gapmers”) 20 nucleotides in length, composed of acentral “gap” region consisting of ten 2′-deoxynucleotides, which isflanked on both sides (5′ and 3′ directions) by five-nucleotide “wings”.The wings are composed of 2′-β-methoxyethyl (2′-MOE) nucleotides. Theinternucleoside (backbone) linkages are phosphorothioate (P═S)throughout the oligonucleotide. All cytidine residues are5-methylcytidines. The compounds were analyzed for their effect on mousediacylglycerol acyltransferase 2 mRNA levels by quantitative real-timePCR as described in other examples herein. Data are averages from threeexperiments in which 3T3-L1 cells were treated with 150 nM of theantisense oligonucleotides of the present invention. If present, “N.D.”indicates “no data”. ISIS 18078 (SEQ ID NO: 2) was used as a negativecontrol in this assay.

TABLE 2 Inhibition of mouse diacylglycerol acyltransferase2 mRNA levels by chimeric phosphorothioateoligonucleotides having 2′-MOE wings and a deoxy gap TARGET SEQ ISISSEQ ID TARGET % ID # REGION NO SITE SEQUENCE (5′ to 3′) INHIB NO 217310Coding 11  555 ctcctgccacctttcttggg  1  20 217312 Coding 11  615tggatgggaaagtagtctcg 59  21 217313 Coding 11  620 ccagctggatgggaaagtag20  22 217314 Coding 11  625 cttcaccagctggatgggaa  0  23 217315 Coding11  630 tgtgtcttcaccagctggat 26  24 217316 Coding 11  635ggttgtgtgtcttcaccagc 46  25 217317 Coding 11  640 cagcaggttgtgtgtcttca36  26 217318 Coding 11  645 gtggtcagcaggttgtgtgt 25  27 217319 Coding11  650 tcctggtggtcagcaggttg 30  28 217320 Coding 11  655atagttcctggtggtcagca 31  29 217321 Coding 11  660 aagatatagttcctggtggt 0  30 217322 Coding 11  665 atccaaagatatagttcctg  0  31 217323 Coding11  670 gtggtatccaaagatatagt 31  32 217324 Coding 11  699aaggcacccaggcccatgat  0  33 217325 Coding 11  822 cctccagacatcaggtactc 2  34 217328 Coding 11  885 gcattgccactcccattctt 37  35 217329 Coding11  890 tgatagcattgccactccca 30  36 217330 Coding 11  895gatgatgatagcattgccac  0  37 217331 Coding 11  900 accacgatgatgatagcatt35  38 217333 Coding 11  939 ttgccaggcatggagctcag 57  39 217336 Coding11 1086 tggacccatcggccccagga  0  40 217337 Coding 11 1091tcttctggacccatcggccc 16  41 217338 Coding 11 1096 gaacttcttctggacccatc34  42 217339 Coding 11 1101 ttctggaacttcttctggac 20  43 217341 Coding11 1173 ggcaccagcccccaggtgtc 14  44 217342 Coding 11 1178agtagggcaccagcccccag  0  45 217343 Coding 11 1183 cttggagtagggcaccagcc18  46 217346 Coding 11 1285 cagggcctccatgtacatgg 36  47 217347 Coding11 1290 ttcaccagggcctccatgta  0  48 217348 Coding 11 1295agagcttcaccagggcctcc 12  49 217353 3′UTR 11 1466 aacccacagacacccatgac  1 50 217354 3′UTR 11 1471 taaataacccacagacaccc 11  51 217355 3′UTR 111476 tcttttaaataacccacaga 19  52 217299 5′UTR 11   21ccaccctagatgagcagaaa  0  98 217300 5′UTR 11   36 ggtaggtagccgctgccacc 26 99 217301 5′UTR 11   44 agagctgaggtaggtagccg 24 100 217302 5′UTR 11  99 gcgctgagctccgggagctg 50 101 217303 5′UTR 11  183aagccaatgcacgtcacggc 18 102 217304 Start Codon 11  199gagggtcttcatgctgaagc 19 103 217305 Coding 11  262 gttttcgctgcgggcagctt10 104 217306 Coding 11  386 gtttttccaccttagatctg  0 105 217307 Coding11  403 tgagatgacctgcagctgtt  0 106 217308 Coding 11  447caggccactcctagcaccag  0 107 217309 Coding 11  457 gatgacactgcaggccactc29 108 217311 Coding 11  586 ccacacggcccagtttcgca 64 109 217326 Coding11  831 gggcagatgcctccagacat 15 110 217327 Coding 11  841tcggttgacagggcagatgc 31 111 217332 Coding 11  920 gggactcagctgcacctccc18 112 217334 Coding 11 1006 cagatcagctccatggcgca 30 113 217335 Coding11 1051 cacctgcttgtatacctcat 41 114 217340 Coding 11 1147gaagaggcctcggccatgga 39 115 217344 Coding 11 1209 ggctcccccacgacggtggt 0 116 217345 Coding 11 1240 ggtcgggtgctccagcttgg 28 117 217349 Coding11 1333 agtctctggaaggccaaatt  3 118 217350 Stop Codon 11 1361ggctgggtcagttcacctcc  0 119 217351 3′UTR 11 1383 ctcccaggagctggcacgcg 47120 217352 3′UTR 11 1424 atgcactcaagaactcggta 60 121 217356 3′UTR 111536 actgactcttcccttcttaa 39 122 217357 3′UTR 11 1560acacactagaagtgagctta 57 123 217358 3′UTR 11 1577 cctccaccttgagcaggaca 45124 217359 3′UTR 11 1599 caccaaggcccataaatatc  6 125 217360 3′UTR 111605 agaaaccaccaaggcccata  0 126 217361 3′UTR 11 1653gccagggccaagtgtctgtc 46 127 217362 3′UTR 11 1685 tggagtcactaaggactgcc 45128 217363 3′UTR 11 1715 gggacatggcctctgcctct  0 129 217364 3′UTR 111746 ggtacgaggaacccgacctg 43 130 217365 3′UTR 11 1772gccagctgtgccctcagcct  0 131 217366 3′UTR 11 1815 ccaagccgggcagtccagat 18132 217367 3′UTR 11 1861 gggtaggctcagattggaga 35 133 217368 3′UTR 111908 cggcacctgtgggacagccg 32 134 217369 3′UTR 11 1946agagtgaaaccagccaacag 23 135 217370 3′UTR 11 2002 gctcaggaggatatgcgcca 90136 217371 3′UTR 11 2033 aagcccttcctcacaccaga  9 137 217372 3′UTR 112055 ggcacctctgtgaagagaag 24 138 217373 3′UTR 11 2086tcctggacccagtgtgctgc 32 139 217374 3′UTR 11 2124 cacacacgtgaggcttggtt 31140 217375 3′UTR 11 2209 atacaaaagtgtgacatggc 30 141 217376 3′UTR 112230 tccatttattagtctaggaa 76 142

As shown in Table 2, SEQ ID Nos: 21, 25, 26, 38, 39, 47, 101, 109, 114,115, 120, 121, 122, 123, 124, 127, 128, 130, 133, 136 and 142demonstrated at least 35% inhibition of mouse diacylglycerolacyltransferase 2 expression in this experiment and are thereforepreferred. More preferred are SEQ ID Nos: 142, 109 and 121. The targetregions to which these preferred sequences are complementary are hereinreferred to as “preferred target segments” and are therefore preferredfor targeting by compounds of the present invention. These preferredtarget segments are shown in Table 3. These sequences are shown tocontain thymine (T) but one of skill in the art will appreciate thatthymine (T) is generally replaced by uracil (U) in RNA sequences. Thesequences represent the reverse complement of the preferred antisensecompounds shown in Tables 1 and 2. “Target site” indicates the first(5′-most) nucleotide number on the particular target nucleic acid towhich the oligonucleotide binds. Also shown in Table 3 is the species inwhich each of the preferred target segments was found.

TABLE 3 Sequence and position of preferred targetsegments identified in diacylglycerol acyltransferase 2. REV COMP TARGETOF SEQ SITE SEQ ID TARGET SEQ ID ID NO SITE SEQUENCE (5′ to 3′) IDACTIVE IN NO 134026  4 579 cccaagaaaggtggcaggag  20 H. sapiens 143134028  4 639 cgagactactttcccatcca  21 H. sapiens 144 134030  4 649ttcccatccagctggtgaag  23 H. sapiens 145 134031  4 654atccagctggtgaagacaca  24 H. sapiens 146 134032  4 659gctggtgaagacacacaacc  25 H. sapiens 147 134033  4 664tgaagacacacaacctgctg  26 H. sapiens 148 134034  4 669acacacaacctgctgaccac  27 H. sapiens 149 134035  4 674caacctgctgaccaccagga  28 H. sapiens 150 134036  4 679tgctgaccaccaggaactat  29 H. sapiens 151 134037  4 684accaccaggaactatatctt  30 H. sapiens 152 134038  4 689caggaactatatctttggat  31 H. sapiens 153 134039  4 694actatatctttggataccac  32 H. sapiens 154 134040  4 723atcatgggcctgggtgcctt  33 H. sapiens 155 134041  4 846gagtacctgatgtctggagg  34 H. sapiens 156 134044  4 909aagaatgggagtggcaatgc  35 H. sapiens 157 134045  4 914tgggagtggcaatgctatca  36 H. sapiens 158 134046  4 919gtggcaatgctatcatcatc  37 H. sapiens 159 134047  4 924aatgctatcatcatcgtggt  38 H. sapiens 160 134049  4 963ctgagctccatgcctggcaa  39 H. sapiens 161 134052  4 1110tcctggggccgatgggtcca  40 H. sapiens 162 134053  4 1115gggccgatgggtccagaaga  41 H. sapiens 163 134054  4 1120gatgggtccagaagaagttc  42 H. sapiens 164 134055  4 1125gtccagaagaagttccagaa  43 H. sapiens 165 134057  4 1197gacacctgggggctggtgcc  44 H. sapiens 166 134058  4 1202ctgggggctggtgccctact  45 H. sapiens 167 134059  4 1207ggctggtgccctactccaag  46 H. sapiens 168 134062  4 1309ccatgtacatggaggccctg  47 H. sapiens 169 134063  4 1314tacatggaggccctggtgaa  48 H. sapiens 170 134064  4 1319ggaggccctggtgaagctct  49 H. sapiens 171 134069  4 1469gtcatgggtgtctgtgggtt  50 H. sapiens 172 134070  4 1474gggtgtctgtgggttattta  51 H. sapiens 173 134071  4 1479tctgtgggttatttaaaaga  52 H. sapiens 174 250517 18 21985tgaggaggatgctcttttgt  53 H. sapiens 175 250518 18 23110tggactgaagcatttatagt  54 H. sapiens 176 250520 18 31611tcccatccaggtaaagtgct  56 H. sapiens 177 250521 18 33686catctgcctcatttcactga  57 H. sapiens 178 250522 18 35303ttgatgtcacctcttttgag  58 H. sapiens 179 250524 18 39106tcccttccagagctgacctg  60 H. sapiens 180 250525 18 37108cccatggaggtccaggggaa  61 H. sapiens 181 250526  4 46ggctgtttctctcgcgccac  62 H. sapiens 182 250527  4 134gctctgcgcgaagccctggc  63 H. sapiens 183 250528  4 222gcttcagccatgaagaccct  64 H. sapiens 184 250529  4 246gccgcctactccggggtcct  65 H. sapiens 185 250530  4 441atctcagtgctccagtgggt  66 H. sapiens 186 250532  4 987gcagtcaccctgcggaaccg  68 H. sapiens 187 250533  4 1387aggtgaactgagccagcctt  69 H. sapiens 188 250534  4 1401agccttcggggccaactccc  70 H. sapiens 189 250535  4 1414aactccctggaggaaccagc  71 H. sapiens 190 250536  4 1449tgctctgtaaatttggaagt  72 H. sapiens 191 250537  4 1584gcttgccctgttctaggtgg  73 H. sapiens 192 250539  4 1647ttcttcccttcctgaagtga  75 H. sapiens 193 250540  4 1679agtcttcttggggaagaagg  76 H. sapiens 194 250541  4 1707tagtgacttggaccagttag  77 H. sapiens 195 250542  4 1724tagatgattcactttttgcc  78 H. sapiens 196 250544  4 1763agccacttctcatacaagcc  80 H. sapiens 197 250545  4 1802acgctcgtctagtcctgaaa  81 H. sapiens 198 250546  4 1946cctagtcactcatatcggag  82 H. sapiens 199 250547  4  1969ggactggcctccaggatgag  83 H. sapiens 200 250548  4 1974ggcctccaggatgaggatgg  84 H. sapiens 201 250549  4 1989gatgggggtggcaatgacac  85 H. sapiens 202 250550  4 2055gccgccaccatgagctaggt  86 H. sapiens 203 250551  4 2067agctaggtggagtaactggt  87 H. sapiens 204 250552  4 2088tttcttgggtggctgatgac  88 H. sapiens 205 250553  4 2125tcagccttggcctggagcac  89 H. sapiens 206 250554  4 2137tggagcacatgcttactggt  90 H. sapiens 207 250555  4 2143acatgcttactggtggcctc  91 H. sapiens 208 250556  4 2150tactggtggcctcagtttac  92 H. sapiens 209 250558  4 2220ggggcctggccttctgagca  94 H. sapiens 210 250559  4 2242agattagttccaaagcaggt  95 H. sapiens 211 250560  4 2269gaacccaagcctcacttttc  96 H. sapiens 212 250561  4 2367ttgcaccatgtcagactttt  97 H. sapiens 213 134018 11 99cagctcccggagctcagcgc 101 M. musculus 214 134027 11 586tgcgaaactgggccgtgtgg 109 M. musculus 215 134051 11 1051atgaggtatacaagcaggtg 114 M. musculus 216 134056 11 1147tccatggccgaggcctcttc 115 M. musculus 217 134067 11 1383cgcgtgccagctcctgggag 120 M. musculus 218 134068 11 1424taccgagttcttgagtgcat 121 M. musculus 219 134072 11 1536ttaagaagggaagagtcagt 122 M. musculus 220 134073 11 1560taagctcacttctagtgtgt 123 M. musculus 221 134074 11 1577tgtcctgctcaaggtggagg 124 M. musculus 222 134077 11 1653gacagacacttggccctggc 127 M. musculus 223 134078 11 1685ggcagtccttagtgactcca 128 M. musculus 224 134080 11 1746caggtcgggttcctcgtacc 130 M. musculus 225 134083 11 1861tctccaatctgagcctaccc 133 M. musculus 226 134086 11 2002tggcgcatatcctcctgagc 136 M. musculus 227 134092 11 2230ttcctagactaataaatgga 142 M. musculus 228

As these “preferred target segments” have been found by experimentationto be open to, and accessible for, hybridization with the antisensecompounds of the present invention, one of skill in the art willrecognize or be able to ascertain, using no more than routineexperimentation, further embodiments of the invention that encompassother compounds that specifically hybridize to these preferred targetsegments and consequently inhibit the expression of diacylglycerolacyltransferase 2.

According to the present invention, antisense compounds includeantisense oligomeric compounds, antisense oligonucleotides, siRNAs,external guide sequence (EGS) oligonucleotides, alternate splicers, andother short oligomeric compounds which hybridize to at least a portionof the target nucleic acid.

Example 17 Western Blot Analysis of Diacylglycerol Acyltransferase 2Protein Levels

Western blot analysis (immunoblot analysis) is carried out usingstandard methods. Cells are harvested 16-20 h after oligonucleotidetreatment, washed once with PBS, suspended in Laemmli buffer (100ul/well), boiled for 5 minutes and loaded on a 16% SDS-PAGE gel. Gelsare run for 1.5 hours at 150 V, and transferred to membrane for westernblotting. Appropriate primary antibody directed to diacylglycerolacyltransferase 2 is used, with a radiolabeled or fluorescently labeledsecondary antibody directed against the primary antibody species. Bandsare visualized using a PHOSPHORIMAGER™ instrument (Molecular Dynamics,Sunnyvale Calif.).

Example 18 Effects of Antisense Inhibition on DiacylglycerolAcyltransferase 2 Levels: In Vivo Studies in a Diet-Induced Model ofObesity

The C57BL/6 mouse strain is reported to be susceptible tohyperlipidemia-induced atherosclerotic plaque formation. Accordingly,these mice were fed a high-fat diet and used in the following studies toevaluate the effects of diacylglycerol acyltransferase 2 antisenseoligonucleotides on mRNA expression in a model of diet-induced obesity.

Male C57BL/6 mice at 6 weeks of age were purchased from JacksonLaboratories (Ben Harbor, Me.). Mice were fed regular rodent chow(#8604, Harlan-Teklad, Madison, Wis.) for 5 days and were subsequentlyplaced on a high-fat diet containing 60% calories from fat (ResearchDiet D12492, Research Diets Inc., New Brunswick, N.J.). After 8 weeks onthe high-fat diet, mice were divided into one of three treatment groupsof eight animals each, based on body weight. One group receivedsubcutaneous injections of ISIS 217376 (SEQ ID No: 142) at a dose of 25mg/kg twice per week for 7 weeks. The second group received subcutaneousinjections of control oligonucleotide ISIS 141923 (CCTTCCCTGAAGGTTCCTCC,SEQ ID NO: 229) at a dose of 25 mg/kg twice per week for 7 weeks.Oligonucleotides were dissolved in 0.9% saline for injection. The thirdgroup received subcutaneous injections of saline twice weekly for 7weeks. This saline-injected group served as the control group to whichthe oligonucleotide-treated groups were compared.

A group of 8 C57B1/6 mice, fed regular rodent chow and treated withsaline, was used as a normal, lean group.

ISIS 141923, which is not complementary to any known gene, is a chimericoligonucleotide (“gapmer”) 20 nucleotides in length, composed of acentral “gap” region consisting of ten 2′-deoxynucleotides, which isflanked on both sides (5′ and 3′ directions) by five-nucleotide “wings”.The wings are composed of 2′-O-methoxyethyl (2′-MOE) nucleotides. Theinternucleoside (backbone) linkages are phosphorothioate (P═S)throughout the oligonucleotide. All cytidine residues are5-methylcytidines.

After the 7 week treatment period, the mice were sacrificed anddiacylglycerol acyltransferase 2 (DGAT2) mRNA levels were evaluated inliver, brown adipose tissue (BAT) and white adipose tissue (\VAT). Inaddition, diacylglycerol acyltransferase 1 (DGAT1) mRNA levels weremeasured in these tissues. mRNA expression levels were quantitated byreal-time PCR as described in other examples herein. The results arepresented in Table 4 and are expressed as percent inhibition relative tosaline-treated mice receiving a high fat diet. A “+” preceding thenumber indicates that gene expression was increased, rather thaninhibited.

TABLE 4 Antisense inhibition of diacylglycerol acyltransferase 2expression in liver, brown adipose and white adipose tissues fromdiet-induced obese mice % Inhibition of diacylglycerol acyltransferasemRNAs Liver WAT BAT DGAT DGAT DGAT DGAT DGAT DGAT ISIS # 2 1 2 1 2 1141923 2 7 +26 +23 25 33 217376 80 47 87 0 78 21

The data demonstrate that diacylglycerol acyltransferase 2 antisenseoligonucleotide treatment can effectively inhibit target mRNA expressionin liver, brown adipose and white adipose tissue. Diacylglycerolacyltransferase 1 expression levels were lowered in liver and brownadipose tissue.

Body weight and food intake were monitored throughout the study.Metabolic rate was measured using indirect calorimetry in a metabolicchamber (Oxymax System, Columbus Instruments, Columbus, Ohio). Adiposetissue weight was also measured at the end of the study. Body weight,adipose tissue weight, food intake and metabolic rate were not changedin diet-induced obese mice treated with ISIS 217376.

In a similar study, animals received twice weekly, subcutaneousinjections of saline, 25 mg/kg ISIS 217376 or 25 mg/kg ISIS 141923, fora period of 5 weeks. In these mice, diacylglycerol acyltransferase 2mRNA was reduced by approximately 90% in liver and white adipose fattissues.

Example 19 Effects of Antisense Inhibition of DiacylglycerolAcyltransferase 2 on Markers of Lipid and Glucose Metabolism

In accordance with the present invention, ISIS 217376 (SEQ ID NO: 142)was tested for its ability to affect lipid and glucose metabolism in thediet-induced obese mice that received antisense oligonucleotidetreatment, as described in Example 18. These mice were further evaluatedat the end of the 7 week treatment period for levels of serum free fattyacids, which were measured using a NEFA C assay kit (part #994-75409,Wako Chemicals, GmbH, Germany). Also measured at the end of the 7 weektreatment period were triglycerides (TRIG), cholesterol, including totalcholesterol (CHOL) and high (HDL) and low (LDL) density lipoproteincholesterol, all of which were measured using the Hitachi 717® analyzerinstrument (Roche Diagnostics, Indianapolis, Ind.). The data, expressedas percent reduction relative to the saline control, are presented inTable 5.

TABLE 5 Effects of antisense inhibition of diacylglycerolacyltransferase 2 on serum cholesterol and lipids in diet-induced obesemice Percent Reduction in Serum Lipids Cholesterol ISIS Free Total HDLLDL # Fatty Acids TRIG CHOL CHOL CHOL 141923 17 13 13 11 30 217376 33 4131 28 24

The results demonstrate that antisense inhibition of diacylglycerolacyltransferase 2 expression, which was presented in Example 18, leadsto significant reductions in of 335, 41% and 31% in serum free fattyacids, serum triglycerides and total cholesterol, respectively.Furthermore, HDL cholesterol was reduced. No significant change wasobserved in LDL cholesterol levels.

Plasma glucose concentrations (n=8 mice) were measured at 0 (beginningof study), 3 and 7 (end of study) weeks of treatment by routine clinicalanalysis using a Y512700 Select™ Biochemistry Analyzer (YSI Inc., YellowSpring, Ohio). Plasma insulin levels (n=6 to 8 mice) were measured inthe fed state at 0, 3 and 7 weeks and following a 4-hour fast at 4weeks, using an insulin ELISA kit (#10-1137-10, ALPCO Diagnostics,Windham, N.H.) according to the manufacturer's instructions. After 4weeks of treatment, an insulin tolerance test (n=8 mice) was performedafter a 3-hour fast. After 5 weeks of treatment, a glucose tolerancetest (n=8 mice) was performed after an overnight fast. For the tolerancetests, a baseline tail blood glucose measurement was obtained, afterwhich 1.0 g/kg glucose or 0.5 units/kg insulin was administeredintraperitoneally. Tail blood glucose levels were measured at 15, 30,60, 90 and 120 minutes following the challenge with glucose or insulin,using a Glucometer® instrument (Abbott Laboratories, Bedford, Mass.).

Treatment with an antisense oligonucleotide targeted to diacylglycerolacyltransferase 2 reduced plasma insulin levels by 50% in the fastedstate at 4 weeks and by 69% in the fed state at the 7 weeks. Plasmaglucose levels were unchanged by treatment with ISIS 217376 indiet-induced obese mice. Neither insulin sensitivity nor glucosetolerance was improved by treatment with ISIS 217376.

Example 20 Effects of Antisense Inhibition of DiacylglycerolAcyltransferase 2 on Hepatic Triglycerides and Steatosis in Diet-InducedObese Mice

In accordance with the present invention, ISIS 217376 (SEQ ID NO: 142)was tested for its ability to affect triglyceride and glycogen contentin the livers of diet-induced obese mice. The diet-induced obese micethat received antisense oligonucleotide treatment, as described inExample 18, were further evaluated at the end of the 7 week treatmentperiod for hepatic triglycerides and glycogen content. Hepatictriglyceride content, which is evaluated by biochemical analysis ofliver triglyceride concentration and histological examination of livertissue, was used to assess hepatic steatosis, or accumulation of lipidsin the liver. To measure liver tissue triglyceride concentration,triglycerides were extracted from liver tissue in HPLC-grade acetone,using a weight:volume ratio of 1:20. Triglycerides were measured usingan Infinity Triglycerides Reagent Kit (Sigma-Aldrich, St. Louis, Mo.).Liver and muscle glycogen concentrations were measured as described byDesai, et al. (Diabetes, 2001, 50, 2287-2295). To measure glycogenconcentrations, liver and muscle tissue were homogenized in 0.03 N HCl(to a final concentration of 0.5 mg/mL). 100 μl of homogenate was mixedwith 400 μL of 1.25 N HCl and heated for 1 hour at 100° C. Followingcentrifugation of the samples at 14,000 rpm, 10 μl of the supernatantwas mixed with 1 mL of glucose oxidase reagent (Sigma-Aldrich, St.Louis, Mo.). After a 10 minute incubation at 37° C., the absorbance wasread at 505 nm. A standard curve was generated using glycogen type IIfrom rabbit liver and used to determine the glycogen concentrations. Thedata for hepatic lipid and glycogen content (n=8 mice) are shown inTable 6 and are expressed as percent reduction relative tosaline-treated, high-fat diet mice.

TABLE 6 Effects of antisense inhibition of diacylglycerolacyltransferase 2 on hepatic lipid and glycogen content Percentreduction in ISIS Hepatic Hepatic # Triglycerides Glycogen 141923 30 5217376 56 3

The results in Table 6 demonstrate that 7 weeks of treatment withantisense oligonucleotide targeted to diacylglycerol acyltransferase 2yields a marked reduction of 56% in hepatic triglyceride contentcompared to saline- and control oligonucleotide-treated mice, indicatingan improvement in hepatic steatosis. Hepatic glycogen content at 7weeks, shown in Table 6, was unchanged by ISIS 217376 treatment.

In the 5-week study, hepatic triglyceride content was lowered by 62% atthe end of the treatment period. Muscle glycogen content after 5 weeksof treatment was unchanged by ISIS 217376 treatment.

The reduction in hepatic triglycerides was also evaluated byhistological examination of liver tissue (n=4 mice). Liver tissue wasfixed in 10% neutral buffered formalin and embedded in paraffin wax.Multiple adjacent 4-um sections were cut and mounted on glass slides.After dehydration, the sections were stained with hematoxylin and eosin,which stain nuclei and cytoplasm, respectively. This histologicalanalysis revealed a marked improvement in hepatic steatosis following 7weeks of treatment with ISIS 217376, as compared to saline-treated orISIS 141923-treated mice. Thus, an improvement in hepatic steatosis wasdemonstrated by both histological and biochemical methods.

Example 21 Effects of Antisense Inhibition of DiacylglycerolAcyltransferase 2 on Hepatic Lipogenic and Gluconeogenic Genes

In accordance with the present invention, ISIS 217376 (SEQ ID NO: 142)was tested for its ability to affect the expression of genes involved infatty acid synthesis and glucose metabolism. The diet-induced obese micethat received antisense oligonucleotide treatment, as described inExample 18, were further evaluated at the end of the 7 week treatmentperiod for expression levels of genes that participate in lipidmetabolism, gluconeogenesis and glucose metabolism. mRNA levels in liverand white adipose tissue were quantitated by real-time PCR as describedin other examples herein, using primer-probe sets that were generatedusing the GenBank® accession numbers provided in Table 7. The resultsare presented as percent change relative to saline-treated, high-fatdiet control mice and are shown in Table 7 (n=6 to 8 mice).

TABLE 7 Lipid and glucose metabolism gene expression following antisenseinhibition of diacylglycerol acyltransferase 2 Percent Change GenBank ®ISIS ISIS Gene Name Accession # 141923 217376 Liver tissue carnitinepalmitoyltransferase I NM_013495.1 −17 −49 acetyl-CoA carboxylase 1NM_000664.1 −18 −66 acetyl-CoA carboxylase 2 NM_001093.1 −5 −90 fattyacid synthase U29344.1 −48 −50 glucose-6-phosphatase, U00445.1 −27 −9catalytic phosphoenolpyruvate NM_011044.1 +14 +23 carboxykinase 1pyruvate kinase NM_013631.1 −47 −73 glucose transporter type 2NM_031197.1 −6 +8 pyruvate dehydrogenase alpha NM_008810.1 −22 −25subunit glycogen phosphorylase AF288783 −2 −19 HMGCoA reductase M62766.1−19 −45 ATP-citrate lyase AF332052 −13 47 Stearoyl-CoA desaturase 1NM_009127 −17 −4 Glycerol kinase NM_008194 −13 −37 Lipoprotein lipaseBC003305.1 +28 +15 sterol regulatory element- AB017337.1 −22 −43 bindingprotein-1 Ppar gamma AB011365.1 −20 −35 White adipose tissue glucosetransporter 4 AB008453.1 +85 +8 glucose transporter type 2 NM_031197.1−7 +3 hormone sensitive lipase U08188.1 +75 +42 lipoprotein lipaseNM_000237.1 +13 −25

These data demonstrate that treatment with ISIS 217376, in addition toreducing the expression of diacylglycerol acyltransferase 2 mRNA indiet-induced obese mice, caused concordant reductions in the expressionof additional genes that participate in lipid metabolism. For example,in liver, decreases were observed in the expression of genes involved intriglyceride synthesis (e.g., glycerol kinase), de novo fatty acidsynthesis (e.g., ATP-citrate lyase, acetyl-CoA carboxylase 1, acetyl-CoAcarboxylase 2 and fatty acid synthase) fatty acid oxidation (e.g.,carnitine palmitoyltransferase I), fatty acid desaturation (e.g.,stearoyl-CoA desaturase 1) and cholesterol synthesis (e.g., HMG-CoAreductase). Furthermore, the expression of glycogen phosphorylase, whichparticipates in glycogen metabolism, was reduced following ISIS 217376treatment of diet-induced obese mice. Lipoprotein lipase, whichparticipates in fatty acid storage in adipose tissue, exhibited reducedexpression as well. The expression of sterol regulatory binding elementprotein 1, which functions as a hepatic transcription factor in thecontext of lipid metabolism, was lowered in diet-induced mice treatedwith ISIS 217376, as compared to control groups. The expression levelsof genes related to gluconeogenesis (e.g., glucose-6-phosphatase andphosphoenolpyruvate carboxykinase 1), glucose uptake in both liver andfat (e.g., glucose transporter type 2 and glucose transporter type 4)and lipid homeostasis in fat (e.g., hormone sensitive lipase andlipoprotein lipase) were not significantly lowered.

These data demonstrate that antisense inhibition of diacylglycerolacyltransferase 2 results in the down-regulation of genes in thelipogenic pathway.

Example 22 Effects of Antisense Inhibition of DiacylglycerolAcyltransferase 2 in the Ob/Ob Mouse Model of Obesity

Leptin is a hormone produced by fat that regulates appetite.Deficiencies in this hormone in both humans and non-human animals leadsto obesity. ob/ob mice have a mutation in the leptin gene which resultsin obesity and hyperglycemia. As such, these mice are a useful model forthe investigation of obesity and treatments designed to reduce obesity.

In accordance with the present invention, the effects of antisenseinhibition of diacylglycerol acyltransferase 2 were investigated in theob/ob mouse model of obesity. Male ob/ob (C57B1/6J-Lep^(ob)/Lep^(ob))mice at 6-7 weeks of age were purchased from Jackson Laboratories (BarHarbor, Me.). During a 1 week acclimation period and throughout thestudy, mice were fed a diet with a fat content of 10-15% (Labdiets#5015, Purina, St. Louis, Mo.). After the 1 week acclimation period,mice were placed into treatment groups based on body weight, as well astail blood glucose, which was measured using a Glucometer® instrument(Abbott Laboratories, Bedford, Mass.) as described herein. For a periodof 4 weeks, mice received subcutaneous, twice-weekly injections of ISIS217376 (SEQ ID NO: 142) or ISIS 116847 (CTGCTAGCCTCTGGATTTGA, SEQ ID NO:230) at a dose of 25 mg/kg. ISIS 116847 does not target thediacylglycerol acyltransferase 2 gene and was used as a control. A groupof saline-injected mice served as the control group to which theoligonucleotide-treated animals were compared. Each group contained 10animals.

ISIS 116847 is a chimeric oligonucleotide (“gapmer”) 20 nucleotides inlength, composed of a central “gap” region consisting of ten2′-deoxynucleotides, which is flanked on both sides (5′ and 3′directions) by five-nucleotide “wings”. The wings are composed of2′-O-methoxyethyl (2′-MOE) nucleotides. The internucleoside (backbone)linkages are phosphorothioate (P═S) throughout the oligonucleotide. Allcytidine residues are 5-methylcytidines. A group of saline-injected miceserved as an untreated control. Each treatment group consisted of 8mice.

At the end of the four week treatment period, the mice were sacrificedand target expression, as well as diacylglycerol acyltransferase 1expression, was measured in liver and fat tissue. mRNA expression wasquantitated by real-time PCR as described in other examples herein.These organs were also weighed. The data are expressed as percentinhibition relative to saline control and are presented in Table 8. A“+” preceding the number indicates that gene expression was increased,rather than inhibited.

TABLE 8 Antisense inhibition of diacylglycerol acyltransferase 2 mRNAexpression in liver and fat tissues from ob/ob mice % Inhibition ofdiacylglycerol acyltransferase mRNAs Liver Fat tissue ISIS # DGAT 2 DGAT1 DGAT 2 DGAT 1 116847 17 11 14 16 217376 83 7 90 +14

The results shown in Table 8 illustrate that treatment of ob/ob micewith ISIS 217376 effectively inhibited, by 83% and 90%, the expressionof target mRNA in both liver and fat tissues, respectively. Liver weightwas reduced by 21% in ob/ob mice treated with the antisenseoligonucleotide of the present invention, but fat tissue weight was notsignificantly changed. No significant reduction in diacylglycerolacyltransferase 1 mRNA expression was observed.

Throughout the study period, body weight and food intake were monitored,however, no changes were observed in ISIS 217376-treated mice relativeto saline-treated mice. Similarly, no change was observed in adiposetissue weight. Metabolic rate, measured as described herein, was alsounchanged following treatment with ISIS 217376.

The expression of genes involved in lipogenesis, for example, fatty acidsynthase, acetyl-CoA carboxylase 1 and acetyl-CoA carboxylase 2, weredecreased following treatment with ISIS 217386.

Example 23 Effects of Antisense Inhibition of DiacylglycerolAcyltransferase 2 in Ob/Ob Mice on Serum and Liver Lipid Content

In accordance with the present invention, ISIS 217376 (SEQ ID NO: 142)was tested for its effect on serum lipids and free fatty acids, as wellas tissue triglyceride levels, in ob/ob mice.

The ob/ob mice that received antisense oligonucleotide treatment, asdescribed in Example 22, were further evaluated at the end of the 4 weektreatment period for serum free fatty acids, serum cholesterol (CHOL),and serum, liver tissue and fat tissue triglycerides (TRIG), all ofwhich were measured as described herein. Hepatic steatosis, oraccumulation of lipids in the liver, was assessed biochemically andhistologically, as described herein. The data describing serum andtissue lipid levels, shown in Table 9, are expressed as percentreduction relative to saline-treated control ob/ob mice. As in Example22, the results are the average of measurements from 8 mice.

TABLE 9 Serum and tissue lipid content following antisense inhibition ofdiacylglycerol acyltransferase 2 % Reduction of serum and tissue lipidcontent Serum Lipids Free Tissue TRIG ISIS # TRIG CHOL Fatty Acids LiverFat 116847 22 10 8 12 14 217376 0 0 22 21 13

The data illustrate that antisense inhibition of diacylglycerolacyltransferase 2 in ob/ob mice causes a reduction of 21% intriglyceride levels in liver tissue and a reduction of 22% in serum freefatty acids. The decrease in liver tissue triglyceride content indicatesan improvement in hepatic steatosis. Furthermore, histologicalevaluation of liver tissue indicated a marked improvement in hepaticsteatosis. No significant change in serum triglyceride, fat tissuetriglyceride or cholesterol was observed.

Example 24 Plasma Insulin and Glucose Levels Following AntisenseInhibition of Diacylglycerolacyltransferase 2 in ob/ob Mice

In accordance with the present invention, the ob/ob mice treated asdescribed in Example 22 were further evaluated for insulin and glucoselevels. Plasma glucose was measured at the start of the antisenseoligonucleotide treatment and after 2 weeks and 4 weeks of treatment.Plasma insulin was measured as described herein following 2 weeks and 4weeks of treatment. After 3 weeks of treatment, glucose and insulintolerance tests were also performed (as described herein) in micefasting for 16 and 4 hours, respectively. Relative to saline-treatedcontrol ob/ob mice, plasma insulin in ob/ob mice receiving ISIS 217376was reduced by 43% at both 2 weeks and 4 weeks of antisenseoligonucleotide treatment. No significant change was observed in plasmaglucose levels, and no improvements in glucose tolerance or insulinsensitivity were observed.

Example 25 Effects of Antisense Inhibition of DiacylglycerolAcyltransferase 2 in the db/db Mouse Model of Obesity

A deficiency in the leptin hormone receptor mice also results in obesityand hyperglycemia. These mice are referred to as db/db mice and, likethe ob/ob mice, are used as a mouse model of obesity.

In accordance with the present invention, antisense inhibition ofdiacylglycerol acyltransferase 2 with ISIS 217276 (SEQ ID NO: 142) wasinvestigated for its effects in db/db mice. Six-week old male db/db(C57B1/6J_Lepr^(db)/Lepr^(db)) mice were fed a 15-20% fat diet (Labdiets#5008, Purina, St. Louis, Mo.) for a 7-day acclimation period andthroughout the study. Following the acclimation period, the mice wereplaced into treatment groups based on body weight, as well as tail bloodglucose, which was measured using a Glucometer® instrument (AbbottLaboratories, Bedford, Mass.) as described herein. Mice receivedsubcutaneous injections of ISIS 217376 (SEQ ID NO: 142) or the controloligonucleotide ISIS 116847 (CTGCTAGCCTCTGGATTTGA, SEQ ID NO: 230) at adose of 25 mg/kg twice per week for 5 weeks. A group of saline-injectedmice served as untreated controls. Each treatment group contained 10mice.

After the 5 week treatment period, mice were sacrificed anddiacylglycerol acyltransferase 2 mRNA levels (n=4 mice) were evaluatedin liver, brown adipose tissue (BAT) and white adipose tissue (WAT).Diacylglycerol acyltransferase 1 mRNA levels were also measured in thesetissues. mRNA expression levels were quantitated by real-time PCR asdescribed in other examples herein. In addition, liver triglycerides(n=6 mice) and plasma glucose (n=8 mice) were measured as describedherein. The results are presented in Table 10 and are expressed aspercent inhibition (for mRNA expression) or reduction (for glucose andtriglycerides) relative to saline treated mice. An increase in geneexpression or liver triglycerides is indicated by a “+” preceding thenumber. Liver tissue samples were processed for histologicalexamination, as described herein, for the evaluation of hepaticsteatosis, or accumulation of lipids in the liver. Liver sections werestained with oil red 0 stain, which is commonly used to visualize lipiddeposits, and counterstained with hematoxylin and eosin, to visualizenuclei and cytoplasm, respectively.

TABLE 10 Effects of antisense inhibition of diacylglycerolacyltransferase 2 in db/db mice Treatment Biological Marker ISIS ISISMeasured 116847 217376 Week % Reduction in 0 0 0 plasma glucose 2 34 5 455 14 % Reduction in 4 +41 41 liver triglycerides mRNA expression intissue % Inhibition Liver +17 95 of diacyglycerol WAT 0 80acyltransferase 2 BAT 19 87 % Inhibition Liver +9 +5 of diacyglycerolWAT +11 5 acyltransferase 1 BAT 13 28

These data illustrate that target mRNA expression was effectivelyinhibited by 95%, 80% and 87% in liver, white adipose and brown adiposetissues, respectively, of db/db mice treated with ISIS 217376.Furthermore, inhibition of diacylglycerol acyltransferase 2 expressionin db/db mice resulted in a 41% reduction in hepatic triglyceridecontent as measured biochemically and marked reductions in lipidaccumulation as measured histologically, demonstrating an improvement inhepatic steatosis. No significant change in plasma glucose was observed.

The expression of genes involved in lipogenesis, for example, fatty acidsynthase, acetyl-CoA carboxylase 1 and acetyl-CoA carboxylase 2 weredecreased following treatment with ISIS 217386.

Together with the data described herein, these data illustrate that theantisense inhibition of diacylglycerol acyltransferase 2 in mouse modelsof diet-induced obesity, leptin deficiency and defects in leptinsignaling reduced hepatic steatosis and hepatic lipogenesis, as well ashyperlipidimia.

Example 26 Design and Screening of siRNAs Targeting Human DiacylglycerolAcyltransferase 2

In a further embodiment, a series of nucleic acid duplexes (siRNAs) wasdesigned to target human diacylglycerol acyltransferase 2 mRNA (SEQ IDNO: 4) and is shown in Table 11. All compounds in Table 11 areoligoribonucleotides 19 nucleotides in length with phosphodiesterinternucleoside linkages (backbones) throughout the compound. Thecompounds were prepared as described herein with blunt ends. Table 11shows the antisense strand of the siRNA, and the sense strand issynthesized as the complement of the antisense strand. These sequencesare shown to contain uracil (U) but one of skill in the art willappreciate that uracil (U) is generally replaced by thymine (T) in DNAsequences. “Target site” indicates the first (5′-most) nucleotide numberon the particular target sequence to which the compound binds.

The compounds in Table 11 were tested for their effects on humandiacylglycerol acyltransferase 2 mRNA levels in A549 cells. siRNAcontrols that do not target human diacylglycerol acyltransferase 2included the duplex of ISIS 335449 (TTTGTCTCTGGTCCTTACTT; incorporatedherein as SEQ ID NO: 231) and its complement, and the duplex of ISIS359661 (TTATCGCTTCTCGTTGCTT; incorporated herein as SEQ ID NO: 232) andits complement. ISIS 335449 is an oligoribonucleotide 20 nucleotides inlength with phosphodiester internucleoside linkages (backbones)throughout the compound. ISIS 359661 is an oligoribonucleotide 19nucleotides in length with phosphodiester internucleoside linkages(backbones) throughout the compound. Both ISIS 335449 and ISIS 359661and their complements were prepared with blunt ends. Control RNase Holigonucleotides were the gapmers ISIS 141923 (SEQ ID NO: 229) and ISIS129700 (TAGTGCGGACCTACCCACGA; incorporated herein as SEQ ID NO: 233),neither of which targets human diacylglycerol acyltransferase 2. ISIS129700 is a chimeric oligonucleotide (“gapmer”) 20 nucleotides inlength, composed of a central “gap” region consisting of 92′-deoxynucleotides, which is flanked on the 5′ and 3′ ends by afive-nucleotide “wing” and a six-nucleotide “wing”, respectively. Thewings are composed of 2′-O-methoxyethyl (2′-MOE) nucleotides. Theinternucleoside (backbone) linkages are phosphorothioate (P═S)throughout the oligonucleotide. All cytidines are 5-methylcytidines.

A549 cells were treated with 150 nM of siRNA compounds mixed with 15μg/mL LIPOFECTINT™ reagent (Invitrogen Corporation, Carlsbad, Calif.) orwith 150 nM of single-strand oligonucleotides mixed with 15 μg/mLLIPOFECTINT™ reagent for a period of 4 hours, followed by 20 hours ofculture in normal growth medium.

Human diacylglycerol acyltransferase 2 mRNA expression was measured byquantitative real-time PCR as described herein. Results were normalizedto untreated control cells, which were not treated with dsRNA compoundsor RNase H oligonucleotides. Data are the average of 2 experiments andare presented in Table 11. Where present, “N.D.” indicates “notdetermined”.

TABLE 11 Inhibition of human diacylglycerol acyltransferase2 mRNA by dsRNAs in A549 cells TARGET SEQ ISIS SEQ ID Target % ID #REGION NO Site SEQUENCE INHIB NO 361884 5′ UTR 4   36GAAACAGCCUAGACCCCAG  0 234 361885 Coding 4  388 AGCCAGGUGACAGAGAAGA 23235 361886 Coding 4  408 UUUCCACCUUGGACCUAUU 24 236 361887 Coding 4  502GUGCAGAAUAUGUACAUGA 22 237 361888 Coding 4  629 GUAGUCUCGAAAGUAGCGC 82238 361889 Coding 4  766 AACUUCUUGCUCACUUCUG 55 239 361890 Coding 4  776UAUGCCUGGGAACUUCUUG 50 240 361891 Coding 4  882 AAUAGUCUAUGGUGUCCCG 66241 361892 Coding 4  892 UUUGAAAGCAAAUAGUCUA 89 242 361893 Coding 4  917GAUGAUAGCAUUGCCACUC 87 243 361894 Coding 4  922 ACGAUGAUGAUAGCAUUGC 44244 361895 Coding 4 1051 CCAAAGGAGUAGAUGGGAA 31 245 361896 Coding 4 1070CUUGUACACUUCAUUCUCU 20 246 361897 Coding 4 1080 AGAUCACCUGCUUGUACAC 52247 361898 Coding 4 1136 ACCAAUGUAUUUCUGGAAC 55 248 361899 Coding 4 1216GUGAUGGGCUUGGAGUAGG  2 249 361900 Coding 4 1320 AGAGCUUCACCAGGGCCUC 36250 361901 Coding 4 1330 UGCUUGUCGAAGAGCUUCA 77 251 361902 Coding 4 1340CUUGGUCUUGUGCUUGUCG 73 252 361903 3′ UTR 4 1459 ACCCAUGACACUUCCAAAU 50253 361904 3′ UTR 4 1500 UUAGCAAAAUUGUUAUAAU  6 254 361905 3′ UTR 4 1510UUGUAAUGGUUUAGCAAAA 42 255 361906 3′ UTR 4 1520 AGACCUAACAUUGUAAUGG N.D.256 361907 3′ UTR 4 1550 UUGAAAUACUGACUUUUUC 55 257 361908 3′ UTR 4 1560GUGAAAGAACUUGAAAUAC 42 258 361909 3′ UTR 4 1570 CAAGCUGGAAGUGAAAGAA 47259 361910 3′ UTR 4 1660 GAGUUUCCUUUGUCACUUC 25 260 361911 3′ UTR 4 1690UAAUGGCAAUCCUUCUUCC 36 261 361912 3′ UTR 4 1900 UCAAACUGGAGCAUUCCAG 55262 361913 3′ UTR 4 1910 AGAAGGGAGAUCAAACUGG 22 263 361914 3′ UTR 4 2076CAAGAAAAACCAGUUACUC  4 264 361915 3′ UTR 4 2231 ACUAAUCUGCUGCUCAGAA 52265 361916 3′ UTR 4 2280 GGAAGGCACAGAAAAGUGA 41 266 361917 3′ UTR 4 2335AGAUAACAGAACACACAGG 24 267 361918 3′ UTR 4 2345 UCUCAUCAAGAGAUAACAG 33268 361919 3′ UTR 4 2355 GGUGCAAUGAUCUCAUCAA 29 269 361920 3′ UTR 4 2380CAAGGCAUAUACAAAAGUC 41 270

These data demonstrated that siRNAs targeted to diacylglycerolacyltransferase 2, for example, duplexes of ISIS 361888, ISIS 361892,ISIS 361893, ISIS 361901 and ISIS 361902, and their respectivecomplements, inhibited expression of the target mRNA.

Example 27 Inhibition of Mouse Diacylglycerol Acyltransferase 2 mRNAExpression in Mouse Primary Hepatocytes: Dose Response Studies

In a further embodiment, four oligonucleotides targeted to mousediacylglycerol acyltransferase 2 were selected for additionaldose-response studies. These compounds were ISIS 217312 (SEQ ID NO: 21),ISIS 217311 (SEQ ID NO: 109), ISIS 217352 (SEQ ID NO: 121), and ISIS217376 (SEQ ID NO: 142). ISIS 129690 (TTAGAATACGTCGCGTTATG, incorporatedherein as SEQ ID NO: 271), and ISIS 129696 (ATTCGCCAGACAACACTGAC,incorporated herein as SEQ ID NO: 272) which are not targeted todiacylglycerol acyltransferase 2, served as controls. ISIS 129690 andISIS 129696 are chimeric oligonucleotides (“gapmers”) 20 nucleotides inlength, composed of a central “gap” region consisting of ten2′-deoxynucleotides, which is flanked on both sides (5′ and 3′directions) by five-nucleotide “wings”. The wings are composed of2′-O-methoxyethyl (2′-MOE) nucleotides. The internucleoside (backbone)linkages are phosphorothioate (P═S) throughout the oligonucleotide. Allcytidine residues are 5-methylcytidines.

Primary mouse hepatocytes were prepared from CD-1 mice purchased fromCharles River Labs (Wilmington, Mass.). Primary mouse hepatocytes wereroutinely cultured in William's Medium E, supplemented with 10% fetalbovine serum, 1% penicillin/streptomycin, 2 mM L-glutamine, and 0.01 MHEPES (medium and supplements from Invitrogen Corporation, Carlsbad,Calif.). Cells were seeded into 96-well plates (Falcon-Primaria #3872,BD Biosciences) coated with 0.1 mg/ml collagen at a density ofapproximately 10,000 cells/well for use in oligonucleotide transfectionexperiments. Cells were transfected using OPTI-MEM™ medium containing2.5 μl per 100 nM of oligonucleotide.

Diacylglycerol acyltransferase 2 mRNA expression was quantitated byreal-time PCR as described herein. Results of these studies are shown inTable 12. Data are averages from three experiments and are expressed aspercent inhibition of untreated control. Also shown is the IC50 for eacholigonucleotide, which represents the concentration required for 50%inhibition of target expression. Where present, “N.D.” indicates notdetermined.

TABLE 12 Inhibition of mouse diacylglycerol acyltransferase 2 mRNAexpression in mouse primary hepatocytes: dose response % Inhibition SEQID Dose of oligonucleotide (nM) IC50 ISIS # NO 6.25 25 100 400 (nM)217311 102 0 1 38 40 406 217312 21 0 10 32 45 407 217352 121 0 27 65 71215 217376 142 0 15 68 91 173 129690 271 9 0 0 0 N.D. 129696 272 0 0 0 0N.D.

As demonstrated in Table 12, ISIS 217311, ISIS 217312, ISIS 217352 andISIS 217376 inhibited diacylglycerol acyltransferase 2 mRNA expressionin a dose-dependent manner.

Example 28 Inhibition of Mouse Diacylglycerol Acyltransferase 2 inPrimary Mouse Hepatocytes: Additional Dose Response Studies

In a further embodiment, an additional antisense compound was designedto target mouse diacylglycerol acyltransferase 2 RNA, using publishedsequence data (GenBank accession number AF384160.1, incorporated hereinas SEQ ID NO: 273). The compound was designated ISIS 287498(ATGCACTCGAGAACTCGGTA, incorporated herein as SEQ ID NO: 274), and thetarget site is nucleotide 1277 of the 3′ UTR region of SEQ ID NO: 4.

ISIS 287498 and ISIS 217352 (SEQ ID NO: 121) were analyzed for theireffects on mouse diacylglycerol acyltransferase 2 mRNA. Controloligonucleotides were ISIS 129686 (CGTTATTAACCTCCGTTGAA, incorporatedherein as SEQ ID NO: 275) and 129690 (SEQ ID NO: 271). ISIS 129686 andISIS 129690 are not targeted to diacylglycerol acyltransferase 2. ISIS129686 and ISIS 287498 are chimeric oligonucleotides (“gapmers”) 20nucleotides in length, composed of a central “gap” region consisting often 2′-deoxynucleotides, which is flanked on both sides (5′ and 3′directions) by five-nucleotide “wings”. The wings are composed of2′-O-methoxyethyl (2′-MOE) nucleotides. The internucleoside (backbone)linkages are phosphorothioate (P═S) throughout the oligonucleotide. Allcytidine residues are 5-methylcytidines.

Primary mouse hepatocytes, isolated and cultured as described in Example27, were treated with 50, 100, 200, and 400 nM of ISIS 287498, ISIS217352, ISIS 129686 and ISIS 129690. Diacylglycerol acyltransferase 2mRNA levels were quantitated by real-time PCR as described herein.Results of these studies are shown in Table 13. Data are averages fromthree experiments and are expressed as percent inhibition normalized toexpression in untreated control cells.

TABLE 13 Inhibition of mouse diacylglycerol acyltransferase 2 mRNAexpression in primary mouse hepatocytes: dose response % Inhibition SEQID Dose of oligonucleotide (nM) ISIS # NO 50 100 200 400 217352 121 5673 84 87 287498 274 61 79 90 89 129686 275 4 0 0 0 129690 271 0 0 0 0

As demonstrated in Table 13, ISIS 217352 and ISIS 287498 inhibiteddiacylglycerol acyltransferase 2 mRNA expression in a dose-dependentmanner.

Example 29 Chimeric Phosphorothioate Oligonucleotides Having 2′-MOEWings and a Deoxy Gap Targeting Human Diacylglycerol Acyltransferase 2

In a further embodiment, an additional series of antisense compounds wasdesigned to target different regions of the human diacylglycerolacyltransferase 2 RNA, using published sequence data (SEQ ID NO: 4 andSEQ ID NO: 18). The compounds are shown in Tables 14 and 15. “Targetsite” indicates the first (5′-most) nucleotide number on the particulartarget sequence to which the compound binds. All compounds in Tables 14and 15 are chimeric oligonucleotides (“gapmers”) 20 nucleotides inlength. The compounds in Table 14 are composed of a central “gap” regionconsisting of ten 2′-deoxynucleotides, which is flanked on both sides(5′ and 3′ directions) by five-nucleotide “wings”. The wings arecomposed of 2′-O-methoxyethyl (2′-MOE) nucleotides. The compounds inTable 15 are composed of a central “gap” region consisting of sixteen2′-deoxynucleotides, which is flanked on both sides (5′ and 3′directions) by two-nucleotide “wings”. The wings are composed of2′-O-methoxyethyl (2′-MOE) nucleotides. In all compounds theinternucleoside (backbone) linkages are phosphorothioate (P═S)throughout the oligonucleotides. All cytidine residues are5-methylcytidines.

TABLE 14 Chimeric phosphorothioate oligonucleotideshaving 5-nucleotide 2′-MOE wings and a 10-nucleotide deoxygap targeted to human diacylglycerol acyltransferase 2 mRNA TARGET SEQISIS SEQ TARGET ID # REGION ID NO SITE SEQUENCE (5′ to 3′) NO 366703 5′UTR 4   75 ACACCTGGAGCTGCGGCCGG 277 366704 5′ UTR 4   80CTAGGACACCTGGAGCTGCG 278 366705 Start Codon 4  229 GGCTATGAGGGTCTTCATGG279 366706 Coding 4  234 TAGGCGGCTATGAGGGTCTT 280 366707 Coding 4  344TGGATCCAGTGCCCCATCTC 281 366708 Coding 4  359 GGGCGGAGAGGATGCTGGAT 282366709 Coding 4  364 CTGGAGGGCGGAGAGGATGC 283 366710 Coding 4  396GACCTATTGAGCCAGGTGAC 284 366711 Coding 4  401 CCTTGGACCTATTGAGCCAG 285366712 Coding 4  406 TTCCACCTTGGACCTATTGA 286 366713 Coding 4  411TGCTTTTCCACCTTGGACCT 287 366714 Coding 4  416 GTAGCTGCTTTTCCACCTTG 288366715 Coding 4  435 TGGAGCACTGAGATGACCTG 289 366716 Coding 4  450AAGGACAGGACCCACTGGAG 290 366717 Coding 4  457 TACAAGGAAGGACAGGACCC 291366718 Coding 4  462 CCCAGTACAAGGAAGGACAG 292 366719 Coding 4  486ATGAGGATGGCACTGCAGGC 293 366720 Coding 4  491 TGTACATGAGGATGGCACTG 294366721 Coding 4  496 GAATATGTACATGAGGATGG 295 366722 Coding 4  501GTGCAGAATATGTACATGAG 296 366723 Coding 4  522 ACAGCGATGAGCCAGCAATC 297366724 Coding 4  528 TAGAGCACAGCGATGAGCCA 298 366725 Coding 4  533TGAAGTAGAGCACAGCGATG 299 366726 Coding 4  538 CCAAGTGAAGTAGAGCACAG 300366727 Coding 4  553 CCAGTCAAACACCAGCCAAG 301 366728 Coding 4  728TGCAGAAGGCACCCAGGCCC 302 366729 Coding 4  766 GAACTTCTTGCTCACTTCTG 303366730 Coding 4  950 AGCTCAGAGACTCAGCCGCA 304 366731 Coding 4  955CATGGAGCTCAGAGACTCAG 305 366732 Coding 4  970 TGCATTCTTGCCAGGCATGG 306366733 Coding 4  980 GCAGGGTGACTGCATTCTTG 307 366734 Coding 4 1002TTCACAAAGCCCTTGCGGTT 308 366735 Coding 4 1069 CTTGTACACTTCATTCTCTC 309366736 Coding 4 1079 AGATCACCTGCTTGTACACT 310 366737 Coding 4 1104CATCGGCCCCAGGAGCCCTC 311 366738 Coding 4 1134 CCAATGTATTTCTGGAACTT 312366739 Coding 4 1139 CGAAACCAATGTATTTCTGG 313 366740 Coding 4 1189CCCCCAGGTGTCGGAGGAGA 314 366741 Coding 4 1216 GGTGATGGGCTTGGAGTAGG 315366742 Coding 4 1293 ATGGTGTGGTACAGGTCGAT 316 366743 Coding 4 1298TGTACATGGTGTGGTACAGG 317 366744 Coding 4 1325 TGTCGAAGAGCTTCACCAGG 318366745 Coding 4 1330 GTGCTTGTCGAAGAGCTTCA 319 366746 Coding 4 1337TGGTCTTGTGCTTGTCGAAG 320 366747 Coding 4 1342 GAACTTGGTCTTGTGCTTGT 321366748 Coding 4 1347 AGGCCGAACTTGGTCTTGTG 322 366749 3′ UTR 4 1513AACATTGTAATGGTTTAGCA 323 366750 3′ UTR 4 1518 GACCTAACATTGTAATGGTT 324366751 3′ UTR 4 1523 AAAAAGACCTAACATTGTAA 325 366752 3′ UTR 4 1591TTAGCCACCACCTAGAACAG 326 366753 3′ UTR 4 1596 CAGATTTAGCCACCACCTAG 327366754 3′ UTR 4 1601 AGGCCCAGATTTAGCCACCA 328 366755 3′ UTR 4 1606AGATTAGGCCCAGATTTAGC 329 366756 3′ UTR 4 1611 CACCCAGATTAGGCCCAGAT 330366757 3′ UTR 4 1616 TGAGCCACCCAGATTAGGCC 331 366758 3′ UTR 4 1621TTAGCTGAGCCACCCAGATT 332 366759 3′ UTR 4 1719 AAAGTGAATCATCTAACTGG 333366760 3′ UTR 4 1808 CTGCAGTTTCAGGACTAGAC 334 366761 3′ UTR 4 1818GAAACTGGTCCTGCAGTTTC 335 366762 3′ UTR 4 1823 GCAGAGAAACTGGTCCTGCA 336366763 3′ UTR 4 1828 CCTTGGCAGAGAAACTGGTC 337 366764 3′ UTR 4 1887ATTCCAGATGCCTACTACTG 338 366765 3′ UTR 4 1892 GGAGCATTCCAGATGCCTAC 339366766 3′ UTR 4 2049 CTCATGGTGGCGGCATCCTC 340 366767 3′ UTR 4 2076CCAAGAAAAACCAGTTACTC 341 366768 3′ UTR 4 2081 GCCACCCAAGAAAAACCAGT 342366769 3′ UTR 4 2096 GCATCCATGTCATCAGCCAC 343

TABLE 15 Chimeric phosphorothioate oligonucleotides having2-nucleotide 2′-MOE wings and a 16-nucleotide deoxy gaptargeted to human diacylglycerol acyltransferase 2 mRNA Target SEQ ISISSEQ TARGET ID # REGION ID NO SITE SEQUENCE (5′ to 3′) NO 370718 5′ UTR 478 AGGACACCTGGAGCTGCGGC 344 370719 Start Codon 4 232GGCGGCTATGAGGGTCTTCA 345 370720 Coding 4 237 GAGTAGGCGGCTATGAGGGT 346370721 Coding 4 249 CGCAGGACCCCGGAGTAGGC 347 370722 Coding 4 347TGCTGGATCCAGTGCCCCAT 348 370723 Coding 4 367 GTCCTGGAGGGCGGAGAGGA 349370724 Coding 4 399 TTGGACCTATTGAGCCAGGT 350 370725 Coding 4 404CCACCTTGGACCTATTGAGC 351 370726 Coding 4 409 CTTTTCCACCTTGGACCTAT 352370727 Coding 4 414 AGCTGCTTTTCCACCTTGGA 353 370728 Coding 4 438CACTGGAGCACTGAGATGAC 354 370729 Coding 4 453 AGGAAGGACAGGACCCACTG 355370730 Coding 4 460 CAGTACAAGGAAGGACAGGA 356 370731 Coding 4 489TACATGAGGATGGCACTGCA 357 370732 Coding 4 494 ATATGTACATGAGGATGGCA 358370733 Coding 4 499 GCAGAATATGTACATGAGGA 359 370734 Coding 4 504TCAGTGCAGAATATGTACAT 360 370735 Coding 4 525 AGCACAGCGATGAGCCAGCA 361370736 Coding 4 531 AAGTAGAGCACAGCGATGAG 362 370737 Coding 4 536AAGTGAAGTAGAGCACAGCG 363 370738 Coding 4 541 CAGCCAAGTGAAGTAGAGCA 364370739 Coding 4 556 GTTCCAGTCAAACACCAGCC 365 370740 Coding 4 657TTGTGTGTCTTCACCAGCTG 366 370741 Coding 4 662 GCAGGTTGTGTGTCTTCACC 367370742 Coding 4 667 GGTCAGCAGGTTGTGTGTCT 368 370743 Coding 4 682GATATAGTTCCTGGTGGTCA 369 370744 Coding 4 769 TGGGAACTTCTTGCTCACTT 370370745 Coding 4 912 ATAGCATTGCCACTCCCATT 371 370746 Coding 4 917TGATGATAGCATTGCCACTC 372 370747 Coding 4 953 TGGAGCTCAGAGACTCAGCC 373370748 Coding 4 958 AGGCATGGAGCTCAGAGACT 374 370749 Coding 4 973GACTGCATTCTTGCCAGGCA 375 370750 Coding 4 983 TCCGCAGGGTGACTGCATTC 376370751 Coding 4 1005 AGTTTCACAAAGCCCTTGCG 377 370752 Coding 4 1072CTGCTTGTACACTTCATTCT 378 370753 Coding 4 1082 CGAAGATCACCTGCTTGTAC 379370754 Coding 4 1107 ACCCATCGGCCCCAGGAGCC 380 370755 Coding 4 1137AAACCAATGTATTTCTGGAA 381 370756 Coding 4 1142 GGGCGAAACCAATGTATTTC 382370757 Coding 4 1192 CAGCCCCCAGGTGTCGGAGG 383 370758 Coding 4 1219AGTGGTGATGGGCTTGGAGT 384 370759 Coding 4 1296 TACATGGTGTGGTACAGGTC 385370760 Coding 4 1301 CCATGTACATGGTGTGGTAC 386 370761 Coding 4 1328GCTTGTCGAAGAGCTTCACC 387 370762 Coding 4 1340 ACTTGGTCTTGTGCTTGTCG 388370763 Coding 4 1345 GCCGAACTTGGTCTTGTGCT 389 370764 Coding 4 1350GGGAGGCCGAACTTGGTCTT 390 370765 3′ UTR 4 1516 CCTAACATTGTAATGGTTTA 391370766 3′ UTR 4 1521 AAAGACCTAACATTGTAATG 392 370767 3′ UTR 4 1594GATTTAGCCACCACCTAGAA 393 370768 3′ UTR 4 1599 GCCCAGATTTAGCCACCACC 394370769 3′ UTR 4 1604 ATTAGGCCCAGATTTAGCCA 395 370770 3′ UTR 4 1609CCCAGATTAGGCCCAGATTT 396 370771 3′ UTR 4 1614 AGCCACCCAGATTAGGCCCA 397370772 3′ UTR 4 1619 AGCTGAGCCACCCAGATTAG 398 370773 3′ UTR 4 1624AGGTTAGCTGAGCCACCCAG 399 370774 3′ UTR 4 1722 CAAAAAGTGAATCATCTAAC 400370775 3′ UTR 4 1811 GTCCTGCAGTTTCAGGACTA 401 370776 3′ UTR 4 1821AGAGAAACTGGTCCTGCAGT 402 370777 3′ UTR 4 1826 TTGGCAGAGAAACTGGTCCT 403370778 3′ UTR 4 1831 TCCCCTTGGCAGAGAAACTG 404 370779 3′ UTR 4 1890AGCATTCCAGATGCCTACTA 405 370780 3′ UTR 4 1895 ACTGGAGCATTCCAGATGCC 406370781 3′ UTR 4 2052 TAGCTCATGGTGGCGGCATC 407 370782 3′ UTR 4 2079CACCCAAGAAAAACCAGTTA 408 370783 3′ UTR 4 2084 TCAGCCACCCAAGAAAAACC 409370784 3′ UTR 4 2099 GCTGCATCCATGTCATCAGC 410 370785 Intron 4 18 33689CTATCAGTGAAATGAGGCAG 411

Example 30 Chimeric Phosphorothioate Oligonucleotides Having 2′-MOEWings and a Deoxy Gap and Targeting Rat Diacylglycerol Acyltransferase 2

In a further embodiment, a series of antisense compounds was designed totarget different regions of the rat diacylglycerol acyltransferase 2RNA, using published sequence data (GenBank accession numberXM_(—)341887.1, incorporated herein as SEQ ID NO: 412, GenBank accessionnumber AA956461.1, the complement of which is incorporated herein as SEQID NO: 413). The compounds are shown in Table 16. “Target site”indicates the first (5′-most) nucleotide number on the particular targetsequence to which the compound binds. All compounds in Table 16 arechimeric oligonucleotides (“gapmers”) 20 nucleotides in length, composedof a central “gap” region consisting of ten 2′-deoxynucleotides, whichis flanked on both sides (5′ and 3′ directions) by five-nucleotide“wings”. The wings are composed of 2′-O-methoxyethyl (2′-MOE)nucleotides. The internucleoside (backbone) linkages arephosphorothioate (P═S) throughout the oligonucleotides. All cytidineresidues are 5-methylcytidines.

TABLE 16 Chimeric phosphorothioate oligonucleotides having2′-MOE wings and a deoxy gap and targeting ratdiacylglycerol acyltransferase 2 mRNA TARGET SEQ ISIS SEQ ID TARGET ID #REGION NO SITE SEQUENCE (5′ to 3′) NO 369163 5′ UTR 412 1CAGAAAGCTAGCGAAGCGCG 414 369164 5′ UTR 412 20 CGCTGCCACCCTAGGCAATC 415369166 5′ UTR 412 40 CGAGATCCGAGGTAGGTAGC 416 369168 5′ UTR 412 60AGGCCGTGGTGGCAGCAGGT 417 369170 5′ UTR 412 80 GGAGCCGAGGGACAGCGCTC 418369172 5′ UTR 412 100 GGGCTTCGCGCTGAGCTCCG 419 369174 5′ UTR 412 124TCCATGCCCCAGCCGCCGGG 420 369176 5′ UTR 412 140 CACGCAGCGCCCCTGATCCA 421369178 5′ UTR 412 160 GGCCGTGCAGGAAGCCGCCT 422 369179 5′ UTR 412 180CTGAAGCCGGTGCACGTCAC 423 369181 5′ UTR 412 198 GCGATGAGGGTCTTCATGCT 424369183 Coding 412 216 AGGACCCCGGAGTAGGCAGC 425 369185 Coding 412 220CCGCAGGACCCCGGAGTAGG 426 369187 Coding 412 240 GCTTCGGCCCGACGCTCACC 427369189 Coding 412 260 TCTTGTTCTCGCTGCGGGCA 428 369191 Coding 412 280TGACAGGGCAGATCCTTTAT 429 369192 Coding 412 300 CATCGCCCAGACCCCTCGCG 430369194 Coding 412 320 GGATGCTGGAGCCAGTGCCC 431 369196 Coding 412 340GATGTCTTGGAGGGCCGAGA 432 369198 Coding 412 360 TTGAGCCAGGTGACAGAGAA 433369200 Coding 412 380 GTTTTTCCACCTTGGATCTG 434 369201 Coding 412 400GACTGAGATGACCTGTAGGT 435 369204 Coding 412 420 AAGGATAGGACCCACTGTAG 436369206 Coding 412 439 GGCCACTCCTAGCACCAGGA 437 369207 Coding 412 460GTACATGAGGATGACACTGC 438 369209 Coding 412 480 CAGCAGTCAGTGCAGAAGGT 439369211 Coding 412 500 AGTAGAGAGCAGCTATCAGC 440 369213 Coding 412 520GTCAAATGCCAGCCAGGTGA 441 369215 Coding 412 540 CCTTTCTTGGGCGTGTTCCA 442369217 Coding 412 560 CCCACTGTGATCTCCTGCCA 443 369218 Coding 412 599AGTAGTCTCGAAAATAGCGC 444 369219 Coding 412 620 TCTTCACCAGCTGGATGGGA 445369220 Coding 412 640 GGTGGTCAGCAGGTTGTGTG 446 369221 Coding 412 660TATCCAAAGATATAGTTCCT 447 369222 Coding 412 685 CAGGCCCATGATGCCATGGG 448369223 Coding 412 700 GTTACAGAAGGCACCCAGGC 449 369224 Coding 412 720TCGGTGGCCTCCGTGCTGAA 450 369225 Coding 412 740 CAGGGAACTTCTTGCTAACT 451369226 Coding 412 761 TGGCCAAATAAGGCCTTATG 452 369227 Coding 412 780CGGAAGTTGCCAGCCAATGT 453 369228 Coding 412 800 ACTCCCGAAGCACAGGCATC 454369229 Coding 412 820 GATGCCTCCAGACATCAGGT 455 369230 Coding 412 840GTGTCTCTGTTGACAGGGCA 456 369231 Coding 412 852 AAGTAGTCTATGGTGTCTCT 457369232 Coding 412 855 AGCAAGTAGTCTATGGTGTC 458 369233 Coding 412 862CTTGGAAAGCAAGTAGTCTA 459 369234 Coding 412 874 ACCACTCCCATTCTTGGAAA 460369235 Coding 413 231 GCATTACCACTCCCATTCTT 461 369236 Coding 412 884CAATGGCATTACCACTCCCA 462 369237 Coding 412 889 GATGACAATGGCATTACCAC 463369238 Coding 412 900 CCTCCCACCACGATGACAAT 464 369239 Coding 412 920AGCTCAGGGATTCAGCTGCA 465 369240 Coding 412 940 TGCGTTCTTGCCAGGCATGG 466369241 Coding 412 960 TTGCGGTTCCGCAGGGTGAC 467 369242 Coding 412 981AGGGCCAGCTTTACAAAGCC 468 369243 Coding 412 1020 CCAAAGGAATAGGTGGGAAC 469369244 Coding 412 1040 GCTTGTATACCTCATTCTCT 470 369245 Coding 412 1059CCCTCCTCAAAGATCACCTG 471 369246 Coding 412 1100 TATACTTCTGGAACTTCTTC 472369247 Coding 412 1112 GGGCGAAACCAATATACTTC 473 369248 Coding 412 1140AAGAGACCTCGGCCATGGAA 474 369249 Coding 412 1160 GCCCCCAGGTGTCAGAGGAG 475369250 Coding 412 1180 GGGCTTGGAGTAGGGCACCA 476 369251 Coding 412 1200TCCCCCACAACGGTGGTGAT 477 369252 Coding 412 1221 AGCTTAGGGACGGTGATGGG 478369253 Coding 412 1241 CTTTCTGGGTCGGGTGCTCC 479 369254 Coding 412 1261GGTGTGGTACAGGTCGATGT 480 369255 Coding 412 1280 CCAGGGCCTCCATGTACATG 481369256 Coding 412 1300 GTGATTGTCAAAGAGCTTCA 482 369257 Coding 412 1320GGAAGGCCGAATTTGGTCTT 483 369258 Coding 412 1340 CCTCCAGCACCTCAGTCTCT 484

Example 31 Design of an Antisense Chimeric PhosphorothioateOligonucleotides Having 2′-MOE Wings and a Deoxy Gap and Targeting MouseDiacylglycerol Acyltransferase 2 Expression

In a further embodiment, an antisense compound ISIS 337205(ATGCACTCAAGAACTCGGTA, incorporated herein as SEQ ID NO: 485) wasdesigned to target the 3′ UTR region of the mouse diacylglycerolacyltransferase 2 RNA, using published sequence data (SEQ ID NO: 11).ISIS 337205 is a chimeric oligonucleotide (“gapmer”) 20 nucleotides inlength, composed of a central “gap” region consisting of 142′-deoxynucleotides, which is flanked on both sides (5′ and 3′directions) by 3-nucleotide “wings”. The wings are composed of2′-O-methoxyethyl (2′-MOE) nucleotides. The internucleoside (backbone)linkages are phosphorothioate (P═S) throughout the oligonucleotide. Allcytidine residues are 5-methylcytidines.

Example 32 Effects of Antisense Inhibition of DiacylglycerolAcyltransferase 2 on Triglyceride Synthesis in Primary RodentHepatocytes

Diacylglycerol acyltransferase 2, which is abundantly expressed in theliver and white adipose tissues, participates in triglyceride synthesisand its activity is also tightly linked to the endogenous fatty acidsynthesis pathway. Thus, it was of interest to determine whetherantisense inhibition of diacylglycerol acyltransferase 2 would affecttriglyceride synthesis in hepatocytes. In a further embodiment, rat andmouse hepatocytes were isolated and treated with ISIS 217357 (SEQ ID NO:123) and ISIS 217376 (SEQ ID NO: 142), respectively. ISIS 217357 is across species oligonucleotide which exhibits 100% complementarity to ratdiacylglycerol acyltransferase 2.

Primary hepatocytes were isolated from C57BL/6J mice or Sprague Dawleyrats (Charles River Laboratories, Wilmington, Mass.). The animals wereanesthetized according to routine procedures. The livers were perfusedvia the portal vein, first with Ca²⁺/Mg²⁺-free Hanks' balanced saltsolution (Invitrogen Corporation, Carlsbad, Calif.) containing 10 mMHepes and 0.5 mM EGTA (pH 7.4) for approximately 3 minutes andsubsequently with digestion buffer (William Medium E, 10 mM Hepes, 2 mMglutamine acid, 0.63 mg/ml collagenase B from Roche, and 0.01 mg/mlgentamycin) for approximately 5 minutes. Perfused livers were removedfrom the mice or rats and dissociated in ice-cold wash buffer (abovedigestion buffer with no collagenase but with addition of 10% fetalbovine serum) by agitation. Parenchymal cells were separated fromnon-parenchymal cells by spinning the harvested cells at 500 rpm for 4min in a CR412™ centrifuge (Jouan Inc, Winchester, Va.). Cells were thenwashed twice with cold PBS. The parenchymal hepatocytes with >85%viability, as assessed by staining with trypan blue, were seeded onto60-mm culture plates coated with collagen type I (BD Biosciences) at1,000,000 cells per plate in culture medium (William Medium E with 10%fetal bovine serum and 10 nm insulin) and cultured overnight at 37° C.and 5% CO₂.

For transfection with antisense oligonucleotides, the culture medium wasaspirated and the hepatocytes were washed once with PBS, andsubsequently incubated for 4-6 hr with 1 ml transfection mixture, whichcontained 150 nM of antisense oligonucleotide and 4.5 μg/mL LIPOFECTINT™reagent (Invitrogen Corporation, Carlsbad, Calif.) in Williams' MediumE. The mixture was then aspirated and replaced with the culture mediumfor approximately 24 hours.

Triglyceride synthesis in transfected hepatocytes was determined bymeasuring the incorporation of tritiated glycerol ([³H]glycerol) intotriglycerides. Approximately 24 hours following transfection, theculture medium was replaced with 1 ml of high glucose DMEM mediumcontaining 10% fetal bovine serum, 0.5% bovine serum albumin (medium andsupplements from Invitrogen Corporation, Carlsbad, Calif.) and 10 uCi of[³H]glycerol with or without 0.5 mM oleate. As oleate is a free fattyacid, and free fatty acids are incorporated into triglycerides duringtriglyceride synthesis, oleate was added to the culture medium of somecells to provide an additional supply of fatty acids and to stimulatetriglyceride synthesis. Insulin, present in the culture medium, is alsoknown to stimulate triglyceride synthesis.

After continued culture overnight, the cells were harvested. One smallfraction of the harvested cells was used for RNA extraction and geneexpression analysis; the remaining fraction was used for lipidextraction with hexane:isopropanol (3:2 in volume) mixture. Theextracted lipids were separated by thin layer chromatography by methodsroutine in the art. The amount of incorporated [³H]glycerol intotriglyceride was determined by liquid scintillation counting. Data arenormalized to untreated control cells and are presented asdisintegrations per minute (DPM) per mg in the cultured cell sample.Tables 17a and 17b show the effects of antisense inhibition ofdiacylglyercol acyltransferase 2 in rat primary hepatocytes and in mouseprimary hepatocytes, respectively.

Real-time PCR quantitation was performed to measure diacylglycerolacyltransferase 2 mRNA levels. Mouse primers and probe used were SEQ IDNOs: 12, 13 and 14. For rat diacylglycerol acyltransferase 2, probes andprimers were designed to hybridize to a rat diacylglycerolacyltransferase 2 sequence, using published sequence information (SEQ IDNO: XM_(—)341887.1, SEQ ID NO: 412). For rat diacylglycerolacyltransferase 2 the PCR primers were:

forward primer: GGAACCGCAAAGGCTTTGTA (SEQ ID NO: 486)reverse primer: AATAGGTGGGAACCAGATCAGC (SEQ ID NO: 487) and the PCRprobe was: FAM-AGCTGGCCCTGCGCCATGG-TAMRA (SEQ ID NO: 488) where FAM isthe fluorescent reporter dye and TAMRA is the quencher dye.

Target expression was normalized to that in cells treated with thecontrol oligonucleotide ISIS 141923.

TABLE 17a Triglyceride synthesis in primary rat hepatocytes Target mRNAMean incorporation of expression [³H]glycerol into SEQ ID (% of ISIStriglycerides ISIS # NO 141923) DPM × 10³/mg protein Without 141923 229100 40 oleate 217357 123 27 8 With 141923 229 100 581 oleate 217357 12323 193

TABLE 17b Triglyceride synthesis in primary mouse hepatocytes TargetmRNA Mean incorporation of expression [³H]glycerol into SEQ ID (% ofISIS triglycerides ISIS # NO 141923) DPM × 10³/mg protein Without 141923229 100 28 oleate 217376 142 25 11 With 141923 229 100 506 oleate 217376142 2 94

These data reveal that the inhibition of diacylglycerol acyltransferase2 in rat hepatocytes dramatically reduced triglyceride synthesis by5-fold and 3-fold in the absence and presence of oleate, respectively.In primary mouse hepatoctyes, triglyceride synthesis was reduced2.5-fold and 5.4-fold in the absence and presence of oleate,respectively, following inhibition of target mRNA expression. Thesereductions occurred regardless of the supply of free fatty acid or theconcentration of insulin in the medium.

The expression levels of lipogenic genes in response to inhibition ofdiacylglycerol acyltransferase 2 were also measured. Real-time PCR wasperformed as described herein, using primer-probe sets designed usingpublished sequence information available from GenBank® database andindicated in Tables 18 and 19. Gene expression levels in primary rathepatocytes and primary mouse hepatocytes were normalized to levels inISIS 141923-treated cells and are shown in Tables 18 and 19,respectively.

TABLE 18 Lipogenic gene expression in primary rat hepatocytes followingtreatment with ISIS 217357 GenBank mRNA expression Target Accession # (%of ISIS 141923) Without Diacylglycerol AF078752.1 150 oleateacyltransferase 1 Stearoyl CoA-desaturase 1 NM_009127 38 Acetyl-CoAcarboxylase 1 BF151634.1 83 Acetyl-CoA carboxylase 2 AF290178.2 44Apolipoprotein C-III L04150.1 111 With Diacylglycerol AF078752.1 96oleate acyltransferase 1 Stearoyl CoA-desaturase 1 NM_009127 56Acetyl-Coa carboxylase 1 BF151634.1 53 Acetyl-CoA carboxylase 2AF290178.2 32 Apolipoprotein C-III L04150.1 94

As shown in Table 18, reductions in the expression of stearoyl-CoAdesaturase 1, acetyl-CoA carboxylase 1 and acetyl-CoA carboxylase 2 wereobserved, both in the presence and absence of oleate. Reductions inthese genes were also observed in vivo following antisense inhibition ofdiacylglycerol acyltransferase 2, as described herein.

TABLE 19 Lipogenic gene expression in primary mouse hepatocytesfollowing treatment with ISIS 217376 GenBank mRNA expression TargetAccession # (% of ISIS 141923) Without Diacylglycerol AF078752.1 95oleate acyltransferase 1 Stearoyl CoA-desaturase 1 NM_009127 77Acetyl-CoA carboxylase 2 AF290178.2 116 With Diacylglycerol AF078752.188 oleate acyltransferase 1

As shown in Table 19, in the absence of oleate, a reduction instearoyl-CoA desaturase 1 was observed in primary mouse hepatocytestreated with ISIS 217376. Reduction in the expression of this gene wasalso observed following treatment of mice with ISIS 217376.

Example 33 Antisense Inhibition of Diacylglycerol Acyltransferase 2 inLean Rats

In a further embodiment, the effects of antisense inhibition ofdiacylglycerol acyltransferase 2 were investigated in normal rats fed alean diet. Male Sprague-Dawley rats, at 6 weeks of age, were purchasedfrom Charles River Laboratories (Wilmington, Mass.). Rats weremaintained on a diet of normal rodent chow (lean diet) and were placedinto one of three treatment groups based on body weight. One treatmentgroup received subcutaneous injections of saline, twice weekly. Twotreatment groups received twice weekly, subcutaneous injections of 50mg/kg oligonucleotide; one group received ISIS 217354 (SEQ ID NO: 51)and the other group received ISIS 217357 (SEQ ID NO: 123). ISIS 217354and ISIS 217357 are cross species oligonucleotides which exhibit 100%complementarity to human, rat and mouse diacylglycerol acyltransferase2.

Rats received a total of 5 doses and were sacrificed 2 days followingthe 5^(th) and final dose of oligonucleotide or saline.

At the end of the study, liver tissue and white adipose tissue (WAT)were collected for quantitative real-time PCR of diacylglycerolacyltransferase 2 mRNA levels. Real-time PCR was performed as describedherein. The data are shown in Table 20, normalized to mRNA expressionlevels in saline-treated mice.

TABLE 20 Antisense inhibition of diacylglycerol acyltransferase 2 mRNAexpression in liver and white adipose tissues from lean rats %Inhibition of diacylglycerol acyltransferase 2 mRNA ISIS # Liver WAT217354 27 14 217357 44 27

These data reveal that ISIS 217354 and ISIS 217357 inhibited theexpression of diacylglycerol acyltransferase 2 mRNA expression in liverand white adipose tissue from lean rats.

Plasma cholesterol and triglycerides were measured by chemical analysisas described herein at the start (t=0 weeks) and end (t=2 weeks) oftreatment. Triglyceride and cholesterol levels are shown as mg/dL inTable 21a.

TABLE 21a Plasma triglyceride and cholesterol levels in lean ratsfollowing antisense inhibition of diacylglycerol acyltransferase 2 Week0 Week 2 Cholesterol Triglycerides Cholesterol Triglycerides ISIS #(mg/dL) (mg/dL) (mg/dL) (mg/dL) Saline 99 46 91 95 217354 90 52 51 36217357 88 68 72 61

As shown in Table 21a, whereas cholesterol and triglycerides in alltreatment groups were similar at the start of treatment, 2 weeks oftreatment with ISIS 217354 or ISIS 217357 resulted in 56% and 79%reductions in plasma cholesterol, respectively and in 38% and 64%reductions in triglycerides, respectively, relative to levels observedin saline-treated mice.

Plasma glucose and insulin were measured as described herein using aYSI2700 Select™ Biochemistry Analyzer and an ELISA kit, respectively, atthe start (t=0 weeks) and end (t=2 weeks) of treatment. In Table 21b,glucose and insulin levels are displayed as mg/dL and ng/mL,respectively.

TABLE 21b Plasma glucose and insulin levels in lean rats followingantisense inhibition of diacylglycerol acyltransferase 2 Week 0 Week 2Glucose Insulin Glucose Insulin ISIS # (mg/dL) (ng/ml) (mg/dL) (ng/ml)Saline 156 .46 134 1.3 217354 139 .41 113 .63 217357 144 .47 132 .78

These data illustrate that while insulin levels in all treatment groupswere similar at t=0 weeks, 2 weeks of treatment with ISIS 217354 or ISIS217357 decreased insulin levels by 52% and 40%, respectively, relativeto those in saline-treated mice. Glucose levels, after 2 weeks oftreatment, were unchanged in oligonucleotide-treated mice relative tosaline-treated mice.

The serum transaminases ALT and AST were measured at the start and endof treatment, by routine analysis using an Olympus Clinical LabAutomation System (Olympus America Inc., Melville, N.Y.). Increases inALT or AST are indicative of treatment-induced toxicity. ALT and ASTlevels are presented in Table 22 in units per liter (U/L).

TABLE 22 Plasma ALT and AST levels Week 0 Week 2 ISIS # ALT (U/L) AST(U/L) ALT (U/L) AST (U/L) Saline 56 104 57 92 217354 55 96 55 60 21735761 94 56 64

The data in Table 22 demonstrate no toxicities resulting from treatmentwith ISIS 217354 and ISIS 217357.

Body weight was monitored throughout the study. As shown in Table 23,increases in body weights were observed in all treatment groups and thuswere not due to treatment with oligonucloetides. No changes wereobserved food intake, which was also monitored throughout the treatmentperiod.

TABLE 23 Body weights in lean rats treated with antisenseoligonucleotides targeting diacylglycerol acyltransferase 2 Week 0 Week1 Week 2 ISIS # Body weight (g) Body weight (g) Body weight (g) Saline192 249 306 217354 194 246 290 217357 193 250 296

These data reveal that antisense oligonucleotides targeted to ratdiacylglycerol acyltransferase 2 effectively inhibited target expressionin lean rats, without causing toxicity. Furthermore, insulin,cholesterol and triglyceride levels were reduced after 2 weeks oftreatment.

Example 34 Antisense Inhibition of Diacylglycerol Acyltransferase 2 in aRat Model of Genetic Obesity

The Zucker fatty (fa/fa) rat is an example of a genetic obesity with anautosomal recessive pattern of inheritance. The obesity in fa/fa animalsis correlated with excessive eating, decreased energy expenditure,compromised thermoregulatory heat production, hyperinsulinemia(overproduction of insulin), and hypercorticosteronemia (overproductionof corticosteroids). The fa mutation has been identified as an aminoacid substitution in the extracellular domain of the receptor forleptin. As a consequence, the fa/fa animal has elevated plasma leptinlevels and is resistant to exogenous leptin administration.

In a further embodiment, the effects of antisense inhibition ofdiacylglycerol acyltransferase 2 are evaluated in the Zucker fa/fa ratmodel of obesity. Male Zucker fa/fa rats, 6 weeks of age, are purchasedfrom Charles River Laboratories (Wilmington, Mass.). Rats are maintainedon a normal rodent diet. Animals are placed into treatments groups of 6animals each. The control group receives twice weekly, subcutaneousinjections of sterile phosphate-buffered saline. Theoligonucleotide-treated groups receive twice weekly, subcutaneousinjections of an antisense oligonucleotide targeted to ratdiacylglycerol acyltransferase 2. By way of example, rats are treatedwith 25, 37.5 or 50 mg/kg of ISIS 217357 (SEQ ID NO: 123). Rats receivea total of 16 to 20 doses over an 8 week period. The rats are sacrificedat the end of the treatment period.

Body weight and food intake are measured at the start of the treatmentperiod and weekly thereafter. Body composition is measured approximately3 days prior to the start of the treatment period and during weeks 2, 4and 5 of treatment.

Serum is collected 2 days prior to the first dose, and every two weeksthereafter. The serum samples, analyzed as described herein, aresubjected to measurements of: the liver transaminases ALT and AST, usingan Olympus Clinical Lab Automation System (Olympus America Inc.,Melville, N.Y.); triglycerides and cholesterol, using the Hitachi 717®analyzer instrument (Roche Diagnostics, Indianapolis, Ind.); free fattyacids, using a NEFA C assay kit (part #994-75409 from Wako Chemicals,GmbH, Germany); and glucose, using a Y512700 Select™ BiochemistryAnalyzer (YSI Inc., Yellow Spring, Ohio). Insulin levels are measuredusing a rat-specific ELISA kit (ALPCO Diagnostics, Windham, N.H.).

To assess the effects of oligonucleotide treatment on glucose tolerance,an oral glucose tolerance test is administered during week 5 and isperformed as described herein.

At the end of the study, liver tissue and epididymal fat tissue arecollected for RNA isolation and quantitative real-time PCR.Diacylglycerol acyltransferase mRNA levels in these tissues are measuredas described herein.

Liver tissue and epididymal fat tissue are also collected for routinehistological analysis. The tissues are first fixed in neutral-bufferedformalin and are subsequently dehydrated, embedded in paraffin wax,sectioned and stained. Hematoxylin and eosin are used to stain nucleiand cytoplasm, respectively, and oil red O is used to visualize lipids.

Liver, spleen, epididymal fat and brown adipose fat tissues are weighedat the end of the study.

The expression levels of genes involved in lipogenic and gluconeogenicpathways in liver and fat tissue are measured using quantitativereal-time PCR. For example, the genes measured are involved intriglyceride synthesis (e.g., glycerol kinase), de novo fatty acidsynthesis (e.g., ATP-citrate lyase, acetyl-CoA carboxylase 1, acetyl-CoAcarboxylase 2 and fatty acid synthase) fatty acid oxidation (e.g.,carnitine palmitoyltransferase I), fatty acid desaturation (e.g.,stearoyl-CoA desaturase 1) and cholesterol synthesis (e.g., HMG-CoAreductase). Furthermore, the expression levels of genes that participatein glycogen metabolism, for example, glycogen phosphorylase, aremeasured. In addition, genes that participate in fatty acid storage, forexample, lipoprotein lipase, are measured. Changes in the expression ofhepatic transcription factors, such as sterol regulatory binding elementprotein 1, are also measured. The expression levels of genes related togluconeogenesis (e.g., glucose-6-phosphatase and phosphoenolpyruvatecarboxykinase 1), glucose uptake in both liver and fat (e.g., glucosetransporter type 2 and glucose transporter type 4) and lipid homeostasisin fat (e.g., hormone sensitive lipase and lipoprotein lipase) are alsomeasured.

Example 35 Antisense Inhibition of Rat Diacylglycerol Acyltransferase 2in Primary Hepatocytes: Dose Response

In a further embodiment, oligonucleotides targeted to rat diacylglycerolacyltransferase 2 were selected for dose response studies in primary rathepatocytes. The oligonucleotides tested were ISIS 217320, ISIS 217336,ISIS 217353, ISIS 217354, ISIS 217356, ISIS 217357 and ISIS 217376.

Primary rat hepatocytes were isolated from Sprague-Dawley rats (CharlesRiver Laboratories, Wilmington, Mass.) and were cultured in WilliamsMedium E supplemented with 10% fetal bovine, 1% penicillin/streptomycin,2 mM L-glutamine, and 0.01 M HEPES (Invitrogen Life Technologies,Carlsbad, Calif.). Cells were seeded into 96-well plates(Falcon-Primaria #3872) coated with 0.1 mg/ml collagen at a density ofapproximately 10,000 cells/well for use in oligonucleotide transfectionexperiments.

Cells were treated with 5, 10, 25, 50, 100 and 200 nM of antisenseoligonucleotide, as described herein. Rat diacylglycerol acyltransferase2 mRNA expression in oligonucleotide-treated cells was measured usingquantitative real-time PCR. The data from the 25, 50, 100 and 200 nMtreatments are averaged from 3 experiments and are shown as percentinhibition, relative to untreated control cells, in Table 24. The 5 and10 nM treatments did not inhibit rat diacylglycerol acyltransferase 2expression.

TABLE 24 Antisense inhibition of diacylglycerol acyltransferase 2 in ratprimary hepatocytes: dose response % Inhibition SEQ ID Dose ofoligonucleotide (nM) ISIS # NO 25 50 100 200 217320 29 0 42 45 27 21733640 17 46 63 72 217353 50 6 60 76 73 217354 51 34 64 66 63 217356 122 047 65 69 217357 123 24 61 75 85 217376 142 0 43 70 81

As shown in Table 24, the oligonucleotides tested in this assayinhibited rat diacylglycerol acyltransferase 2 expression in primaryhepatocytes. ISIS 217336, ISIS 217353, ISIS 217356, ISIS 217357 and ISIS217376 inhibited target mRNA expression in a dose-dependent manner.

All publications cited in this specification are incorporated byreference herein. While the invention has been described with referenceto a particularly preferred embodiment, it will be appreciated thatmodifications can be made without departing from the spirit of theinvention. Such modifications are intended to fall within the scope ofthe appended claims.

What is claimed is:
 1. An antisense compound 13 to 40 nucleobases inlength targeted to a target segment of a nucleic acid molecule encodingdiacylglycerol acyltransferase 2 (SEQ ID NO: 4), the target segmentcomprising nucleotides 909 to 943, nucleotides 909 to 1134, nucleotides654 to 688, nucleotides 654 to 698, nucleotides 654 to 713, nucleotides1197 to 1226, nucleotides 1309 to 1496, nucleotides 1197 to 1406,nucleotides 1309 to 1468, nucleotides 1197 to 1468, nucleotides 1707 to1743, nucleotides 1763 to 1821, nucleotides 1946 to 1988, nucleotides2067 to 2169 or nucleotides 2220 to 2261 and wherein said compound is achimeric oligonucleotide comprising at least one phosphorothioateinternucleotide linkage and at least one 2′-O -methoxyethyl modifiedsugar moiety.
 2. The antisense compound of claim 1 comprising 15 to 30nucleobases in length.
 3. The antisense compound of claim 1 having atleast 95% complementarity with said target segment.
 4. The antisensecompound of claim 1 having at least 99% complementarity with said targetsegment.
 5. A method of ameliorating or lessening the severity of acondition in an animal comprising contacting said animal with aneffective amount of the compound of claim 1 so that expression ofdiacylglycerol acyltransferase 2 is inhibited and measurement of one ormore physical indicia of said condition indicates a lessening of theseverity of said condition.
 6. The method of claim 5 wherein thecondition is a cardiovascular disorder, obesity, diabetes,cholesterolemia, or liver steatosis.
 7. The method of claim 6 whereinthe obesity is diet-induced.
 8. The method of claim 6 wherein physicalindicia of obesity is increased fat.
 9. The method of claim 5 whereinthe animal is a mammal.
 10. The method of claim 6, wherein the liversteatosis is steatohepatitis, non-alcoholic fatty liver disease ornon-alcoholic steatohepatitis (NASH).
 11. A method of lowering serumfree fatty acids, serum triglycerides, HDL cholesterol, total serumcholesterol, VLDL cholesterol, plasma insulin, serum insulin, hepatictriglycerides, plasma apolipoprotein B level or a combination thereof inan animal comprising administering to said animal an antisense compoundof claim
 1. 12. The method of claim 11, further comprising the step ofselecting an animal in need of such treatment.
 13. A method ofincreasing insulin sensitivity or leptin sensitivity in an animalcomprising administering to said animal an antisense oligonucleotide ofclaim
 1. 14. The method of claim 13, further comprising the step ofselecting an animal in need of such treatment.
 15. An antisense compoundof claim 1, wherein the antisense compound is 20 nucleobases in length.16. An antisense compound of claim 15, wherein all internucleotidelinkages are phosphorothioates and at least one 2-O-methoxyethylnucleotide is at each of the 3′ and 5′ termini of said antisensecompound.
 17. An antisense compound of claim 16, wherein nucleotides 1-5are 2-O-methoxyethyl nucleotides, nucleotides 6-15 are2-deoxynucleotides, and nucleotides 16-20 are 2-O-methoxyethylnucleotides.
 18. An antisense compound of claim 16, wherein nucleotides1-2 are 2-O-methoxyethyl nucleotides, nucleotides 3-18 are2-deoxynucleotides, and nucleotides 19-20 are 2-O-methoxyethylnucleotides.
 19. The method of claim 11 wherein lowering serum freefatty acids, serum triglycerides, HDL cholesterol, total serumcholesterol, VLDL cholesterol, plasma insulin, serum insulin, hepatictriglycerides, plasma apolipoprotein B level or a combination thereofreduces an animal's risk of developing cardiovascular disease.
 20. Themethod of claim 11 wherein lowering serum free fatty acids, serumtriglycerides, HDL cholesterol, total serum cholesterol, VLDLcholesterol, plasma insulin, serum insulin, hepatic triglycerides,plasma apolipoprotein B level or a combination thereof improves ananimal's cardiovascular risk profile.
 21. The method of claim 11 whereinlowering serum free fatty acids, serum triglycerides, HDL cholesterol,total serum cholesterol, VLDL cholesterol, plasma insulin, seruminsulin, hepatic triglycerides, plasma apolipoprotein B level or acombination thereof ameliorates or lessens the severity of a conditionassociated with an increased cardiovascular risk profile.
 22. The methodof claim 12 wherein the cardiovascular risk profile of the animal isimproved.